Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Sørensen, Karina Meden
Andersen, Paal Skytt
Larsen, Lars Allan
Schwartz, Marianne
Schouten, Jan P.
and
Nygren, Anders O. H.
2008.
Multiplex Ligation-Dependent Probe Amplification Technique for Copy Number Analysis on Small Amounts of DNA Material.
Analytical Chemistry,
Vol. 80,
Issue. 23,
p.
9363.
Watanabe, Takashi
Tanaka, Gotaro
Hamada, Shuichi
Namiki, Chiaki
Suzuki, Takayoshi
Nakajima, Madoka
and
Furihata, Chie
2009.
Dose-dependent alterations in gene expression in mouse liver induced by diethylnitrosamine and ethylnitrosourea and determined by quantitative real-time PCR.
Mutation Research/Genetic Toxicology and Environmental Mutagenesis,
Vol. 673,
Issue. 1,
p.
9.
Saxena, Kapil
Kitzmiller, Kathryn J.
Wu, Yee Ling
Zhou, Bi
Esack, Nazreen
Hiremath, Leena
Chung, Erwin K.
Yang, Yan
and
Yu, C. Yung
2009.
Great genotypic and phenotypic diversities associated with copy-number variations of complement C4 and RP-C4-CYP21-TNX (RCCX) modules: A comparison of Asian-Indian and European American populations.
Molecular Immunology,
Vol. 46,
Issue. 7,
p.
1289.
Choi, Jin-Ho
Kim, Gu-Hwan
and
Yoo, Han-Wook
2010.
Molecular Genetic Diagnosis of Genetic Endocrine Diseases.
Journal of Genetic Medicine,
Vol. 7,
Issue. 1,
p.
16.
McNicol, Anne Marie
2010.
Molecular Pathology of Endocrine Diseases.
Vol. 3,
Issue. ,
p.
213.
MAITRA, ANIRBAN
2010.
Robbins and Cotran Pathologic Basis of Disease.
p.
1097.
Paller, Amy S.
and
Mancini, Anthony J.
2011.
Hurwitz Clinical Pediatric Dermatology.
p.
528.
Vrzalová, Zuzana
Hrubá, Zuzana
Hrabincová, Eva Sťahlová
Vrábelová, Slávka
Votava, Felix
Koloušková, Stanislava
and
Fajkusová, Lenka
2011.
Chimeric CYP21A1P/CYP21A2 genes identified in Czech patients with congenital adrenal hyperplasia.
European Journal of Medical Genetics,
Vol. 54,
Issue. 2,
p.
112.
Rabbani, Bahareh
Mahdieh, Nejat
Ashtiani, Mohammad Tahgi Haghi
Larijani, Bagher
Akbari, Mohammad Taghi
New, Maria
Parsa, Alan
Schouten, Jan P.
and
Rabbani, Ali
2012.
Mutation Analysis of theCYP21A2Gene in the Iranian Population.
Genetic Testing and Molecular Biomarkers,
Vol. 16,
Issue. 2,
p.
82.
Bertholf, Roger L.
Jialal, Ishwarlal
and
Winter, William E.
2012.
Tietz Textbook of Clinical Chemistry and Molecular Diagnostics.
p.
1847.
Toraman, Bayram
Ökten, Ayşenur
Kalay, Ersan
Karagüzel, Gülay
Dinçer, Tuba
Açıkgöz, Emel Gül
and
Karagüzel, Ahmet
2013.
Investigation of CYP21A2 mutations in Turkish patients with 21-hydroxylase deficiency and a novel founder mutation.
Gene,
Vol. 513,
Issue. 1,
p.
202.
McNicol, Anne Marie
2013.
Diagnostic and molecular aspects of adrenal cortical tumors.
Seminars in Diagnostic Pathology,
Vol. 30,
Issue. 3,
p.
197.
Milacic, I.
Barac, M.
Milenkovic, T.
Ugrin, M.
Klaassen, K.
Skakic, A.
Jesic, M.
Joksic, I.
Mitrovic, K.
Todorovic, S.
Vujovic, S.
Pavlovic, S.
and
Stojiljkovic, M.
2015.
Molecular genetic study of congenital adrenal hyperplasia in Serbia: novel p.Leu129Pro and p.Ser165Pro CYP21A2 gene mutations.
Journal of Endocrinological Investigation,
Vol. 38,
Issue. 11,
p.
1199.
Charni, M
Molchadsky, A
Goldstein, I
Solomon, H
Tal, P
Goldfinger, N
Yang, P
Porat, Z
Lozano, G
and
Rotter, V
2016.
Novel p53 target genes secreted by the liver are involved in non-cell-autonomous regulation.
Cell Death & Differentiation,
Vol. 23,
Issue. 3,
p.
509.
Paller, Amy S.
and
Mancini, Anthony J.
2016.
Hurwitz Clinical Pediatric Dermatology.
p.
540.
Khajuria, Ragini
Walia, Rama
Bhansali, Anil
and
Prasad, Rajendra
2017.
The spectrum of CYP21A2 mutations in Congenital Adrenal Hyperplasia in an Indian cohort.
Clinica Chimica Acta,
Vol. 464,
Issue. ,
p.
189.
Anastasovska, Violeta
Kocova, Mirjana
Zdraveska, Nikolina
Stojiljkovic, Maja
Skakic, Anita
Klaassen, Kristel
and
Pavlovic, Sonja
2021.
A novel 9 bp deletion (c.1271_1279delGTGCCCGCG) in exon 10 of CYP21A2 gene causing severe congenital adrenal hyperplasia.
Endocrine,
Vol. 73,
Issue. 1,
p.
196.
Carvalho, Berta
Carvalho, Filipa
and
Carvalho, Davide
2024.
Adrenal Glands - The Current Stage and New Perspectives of Diseases and Treatment.