Mutation analysis of the CYP21A2 gene in the Iranian population.
about
Genotype-phenotype correlation in 1,507 families with congenital adrenal hyperplasia owing to 21-hydroxylase deficiencyPitfalls in molecular diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasiaA CYP21A2 gene mutation in patients with congenital adrenal hyperplasia. Molecular genetics report from Saudi Arabia.Clinical profile and inheritance pattern of CYP21A2 gene mutations in patients with classical congenital adrenal hyperplasia from 10 families.21-hydroxylase deficiency: newborn screening in iran?Mutation detection of CYP21A2 gene in nonclassical congenital adrenal hyperplasia patients with premature pubarche.
P2860
Mutation analysis of the CYP21A2 gene in the Iranian population.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Mutation analysis of the CYP21A2 gene in the Iranian population.
@ast
Mutation analysis of the CYP21A2 gene in the Iranian population.
@en
type
label
Mutation analysis of the CYP21A2 gene in the Iranian population.
@ast
Mutation analysis of the CYP21A2 gene in the Iranian population.
@en
prefLabel
Mutation analysis of the CYP21A2 gene in the Iranian population.
@ast
Mutation analysis of the CYP21A2 gene in the Iranian population.
@en
P2093
P2860
P356
P1476
Mutation analysis of the CYP21A2 gene in the Iranian population.
@en
P2093
Alan Parsa
Ali Rabbani
Bahareh Rabbani
Jan P Schouten
Mohammad Taghi Akbari
Mohammad Tahgi Haghi Ashtiani
Nejat Mahdieh
P2860
P356
10.1089/GTMB.2011.0099
P577
2011-10-21T00:00:00Z