Crossref Citations
                  
                    
                    
                      
                        This article has been cited by the following publications. This list is generated based on data provided by 
    Crossref.
                     
                   
                  
                        
                          
                                
                                
                                    
                                    Laarabi, F
                                    
                                    Jaouad, I
                                    
                                    El Kerch, F
                                     and 
                                    Sefiani, A
                                  2009.
                                  MYH Associated Polyposis with a p.Tyr165Cys Mutation in a Moroccan Patient.
                                  
                                  
                                  Balkan Journal of Medical Genetics, 
                                  Vol. 12, 
                                  Issue. 2, 
                                
                                    p. 
                                    65.
                                
                                
                        
                        
                        
                        
      
                          
                                
                                
                                    
                                    Borhany, Munira
                                    
                                    Pahore, Zaen
                                    
                                    ul Qadr, Zeeshan
                                    
                                    Rehan, Muhammad
                                    
                                    Naz, Arshi
                                    
                                    Khan, Asif
                                    
                                    Ansari, Saqib
                                    
                                    Farzana, Tasneem
                                    
                                    Nadeem, Muhammad
                                    
                                    Raza, Syed Amir
                                     and 
                                    Shamsi, Tahir
                                  2010.
                                  Bleeding disorders in the tribe: result of consanguineous in breeding.
                                  
                                  
                                  Orphanet Journal of Rare Diseases, 
                                  Vol. 5, 
                                  Issue. 1, 
                                
                                
                                
                        
                        
                        
                        
      
                          
                                
                                
                                    
                                    Sefiani, Abdelaziz
                                  2010.
                                  Genetic Disorders Among Arab Populations.
                                  
                                  
                                  
                                  
                                  
                                
                                    p. 
                                    455.
                                
                                
                        
                        
                        
                        
      
                          
                                
                                
                                    
                                    Wahabi, Hayfaa A
                                    
                                    Alzeidan, Rasmeia A
                                    
                                    Bawazeer, Ghada A
                                    
                                    Alansari, Lubna A
                                     and 
                                    Esmaeil, Samia A
                                  2010.
                                  Preconception care for diabetic women for improving maternal and fetal outcomes: a systematic review and meta-analysis.
                                  
                                  
                                  BMC Pregnancy and Childbirth, 
                                  Vol. 10, 
                                  Issue. 1, 
                                
                                
                                
                        
                        
                        
                        
      
                          
                                
                                
                                    
                                    Shawky, Rabah M.
                                     and 
                                    Sadik, Doaa I.
                                  2011.
                                  Congenital malformations prevalent among Egyptian children and associated risk factors.
                                  
                                  
                                  Egyptian Journal of Medical Human Genetics, 
                                  Vol. 12, 
                                  Issue. 1, 
                                
                                    p. 
                                    69.
                                
                                
                        
                        
                        
                        
      
                          
                                
                                
                                    
                                    la Marca, Giancarlo
                                    
                                    Malvagia, Sabrina
                                    
                                    Pasquini, Elisabetta
                                    
                                    Cavicchi, Catia
                                    
                                    Morrone, Amelia
                                    
                                    Ciani, Federica
                                    
                                    Funghini, Silvia
                                    
                                    Villanelli, Fabio
                                    
                                    Zammarchi, Enrico
                                     and 
                                    Guerrini, Renzo
                                  2011.
                                  JIMD Reports - Case and Research Reports, 2011/1.
                                  
                                  
                                  
                                  Vol. 1, 
                                  Issue. , 
                                
                                    p. 
                                    107.
                                
                                
                        
                        
                        
                        
      
                          
                                
                                
                                    
                                    Sbiti, A.
                                    
                                    Ratbi, I.
                                    
                                    Kriouile, Y.
                                     and 
                                    Sefiani, A.
                                  2011.
                                  L’amyotrophie spinale infantile : cause fréquente des hypotonies congénitales au Maroc.
                                  
                                  
                                  Archives de Pédiatrie, 
                                  Vol. 18, 
                                  Issue. 12, 
                                
                                    p. 
                                    1261.
                                
                                
                        
                        
                        
                        
      
                          
                                
                                
                                    
                                    Laarabi, F. Z.
                                    
                                    Cherkaoui Jaouad, I.
                                    
                                    Benazzouz, A.
                                    
                                    Squalli, D.
                                     and 
                                    Sefiani, A.
                                  2011.
                                  Prevalence of MYH-associated polyposis related to three recurrent mutations in Morocco.
                                  
                                  
                                  Annals of Human Biology, 
                                  Vol. 38, 
                                  Issue. 3, 
                                
                                    p. 
                                    360.
                                
                                
                        
                        
                        
                        
      
                          
                                
                                
                                    
                                    El Kerch, F.
                                    
                                    Lamzouri, A.
                                    
                                    Laarabi, F.Z.
                                    
                                    Zahi, M.
                                    
                                    Ben Amar, B.
                                     and 
                                    Sefiani, A.
                                  2011.
                                  Confirmation de la forte prévalence au Maroc de la mutation homozygote c.144delC du gène aurora kinase C (AURKC) dans les tératozoospermies avec spermatozoïdes macrocéphales.
                                  
                                  
                                  Journal de Gynécologie Obstétrique et Biologie de la Reproduction, 
                                  Vol. 40, 
                                  Issue. 4, 
                                
                                    p. 
                                    329.
                                
                                
                        
                        
                        
                        
      
                          
                                
                                
                                    
                                    AL-KANDARI, YAGOUB Y.
                                     and 
                                    CREWS, DOUGLAS E.
                                  2011.
                                  THE EFFECT OF CONSANGUINITY ON CONGENITAL DISABILITIES IN THE KUWAITI POPULATION.
                                  
                                  
                                  Journal of Biosocial Science, 
                                  Vol. 43, 
                                  Issue. 1, 
                                
                                    p. 
                                    65.
                                
                                
                        
                        
                        
                        
      
                          
                                
                                
                                    
                                    Cauchi, S.
                                    
                                    Ezzidi, I.
                                    
                                    El Achhab, Y.
                                    
                                    Mtiraoui, N.
                                    
                                    Chaieb, L.
                                    
                                    Salah, D.
                                    
                                    Nejjari, C.
                                    
                                    Labrune, Y.
                                    
                                    Yengo, L.
                                    
                                    Beury, D.
                                    
                                    Vaxillaire, M.
                                    
                                    Mahjoub, T.
                                    
                                    Chikri, M.
                                     and 
                                    Froguel, P.
                                  2012.
                                  European genetic variants associated with type 2 diabetes in North African Arabs.
                                  
                                  
                                  Diabetes & Metabolism, 
                                  Vol. 38, 
                                  Issue. 4, 
                                
                                    p. 
                                    316.
                                
                                
                        
                        
                        
                        
      
                          
                                
                                
                                    
                                    DOUBAJ, Yassamine
                                    
                                    LAARABI, Fatima‐Zahra
                                    
                                    CHAFAI ELALAOUI, Siham
                                    
                                    BARKAT, Amina
                                     and 
                                    SEFIANI, Abdelaziz
                                  2012.
                                  Carrier frequency of the recurrent mutation c.1643_1644delTG in the XPC gene and birth prevalence of the xeroderma pigmentosum in Morocco.
                                  
                                  
                                  The Journal of Dermatology, 
                                  Vol. 39, 
                                  Issue. 4, 
                                
                                    p. 
                                    382.
                                
                                
                        
                        
                        
                        
      
                          
                                
                                
                                    
                                    Belmahi, Latifa
                                    
                                    Cherkaoui, Imane Jaouad
                                    
                                    Hama, Iman
                                     and 
                                    Sefiani, Abdelaziz
                                  2012.
                                  MEFV mutations in Moroccan patients suffering from familial Mediterranean Fever.
                                  
                                  
                                  Rheumatology International, 
                                  Vol. 32, 
                                  Issue. 4, 
                                
                                    p. 
                                    981.
                                
                                
                        
                        
                        
                        
      
                          
                                
                                
                                    
                                    Tajir, Mariam
                                    
                                    Arnoux, Jean Baptiste
                                    
                                    Boutron, Audrey
                                    
                                    Elalaoui, Siham Chafai
                                    
                                    De Lonlay, Pascale
                                    
                                    Sefiani, Abdelaziz
                                     and 
                                    Brivet, Michèle
                                  2012.
                                  Pyruvate dehydrogenase deficiency caused by a new mutation of PDHX gene in two Moroccan patients.
                                  
                                  
                                  European Journal of Medical Genetics, 
                                  Vol. 55, 
                                  Issue. 10, 
                                
                                    p. 
                                    535.
                                
                                
                        
                        
                        
                        
      
                          
                                
                                
                                    
                                    Lamzouri, Afaf
                                    
                                    Ratbi, Ilham
                                    
                                    Laarabi, Fatima Z.
                                    
                                    Barkat, Amina
                                     and 
                                    Sefiani, Abdelaziz
                                  2012.
                                  Low Prevalence of p.G352fsdelG Mutation in Phenylketonuria Patients from Morocco.
                                  
                                  
                                  Genetic Testing and Molecular Biomarkers, 
                                  Vol. 16, 
                                  Issue. 8, 
                                
                                    p. 
                                    996.
                                
                                
                        
                        
                        
                        
      
                          
                                
                                
                                    
                                    Hama, I.
                                    
                                    Ratbi, I.
                                    
                                    Reggoug, S.
                                    
                                    Elkerch, F.
                                    
                                    Kharrasse, G.
                                    
                                    Errabih, I.
                                    
                                    Ouazzani, H.
                                     and 
                                    Sefiani, A.
                                  2012.
                                  Non-association of Crohn's disease with NOD2 gene variants in Moroccan patients.
                                  
                                  
                                  Gene, 
                                  Vol. 499, 
                                  Issue. 1, 
                                
                                    p. 
                                    121.
                                
                                
                        
                        
                        
                        
      
                          
                                
                                
                                    
                                    Wahabi, Hayfaa A
                                    
                                    Alzeidan, Rasmieh A
                                     and 
                                    Esmaeil, Samia A
                                  2012.
                                  Pre-pregnancy care for women with pre-gestational diabetes mellitus: a systematic review and meta-analysis.
                                  
                                  
                                  BMC Public Health, 
                                  Vol. 12, 
                                  Issue. 1, 
                                
                                
                                
                        
                        
                        
                        
      
                          
                                
                                
                                    
                                    Assady, Suheir
                                    
                                    Ramadan, Rawi
                                     and 
                                    Rubinger, Dvora
                                  2012.
                                  Brenner and Rector's The Kidney.
                                  
                                  
                                  
                                  
                                  
                                
                                    p. 
                                    2744.
                                
                                
                        
                        
                        
                        
      
                          
                                
                                
                                    
                                    Lyahyai, Jaber
                                    
                                    Sbiti, Aziza
                                    
                                    Barkat, Amina
                                    
                                    Ratbi, Ilham
                                     and 
                                    Sefiani, Abdelaziz
                                  2012.
                                  Spinal Muscular Atrophy Carrier Frequency and Estimated Prevalence of the Disease in Moroccan Newborns.
                                  
                                  
                                  Genetic Testing and Molecular Biomarkers, 
                                  Vol. 16, 
                                  Issue. 3, 
                                
                                    p. 
                                    215.
                                
                                
                        
                        
                        
                        
      
                          
                                
                                
                                    
                                    Laarabi, F.Z.
                                    
                                    Cherkaoui Jaouad, I.
                                    
                                    Baert-Desurmont, S.
                                    
                                    Ouldim, K.
                                    
                                    Ibrahimi, A.
                                    
                                    Kanouni, N.
                                    
                                    Frebourg, T.
                                     and 
                                    Sefiani, A.
                                  2012.
                                  The first mutations in the MYH gene reported in Moroccan colon cancer patients.
                                  
                                  
                                  Gene, 
                                  Vol. 496, 
                                  Issue. 1, 
                                
                                    p. 
                                    55.