Molecular Diagnosis of Congenital Adrenal Hyperplasia in Iran: Focusing on CYP21A2 Gene.

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21-hydroxylase deficiency: newborn screening in iran?Molecular Analysis of CYP21A2 Gene Mutations among Iraqi Patients with Congenital Adrenal Hyperplasia.An overview of mutation detection methods in genetic disorders.

P2860

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Molecular Diagnosis of Congenital Adrenal Hyperplasia in Iran: Focusing on CYP21A2 Gene.

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2011 nî lūn-bûn

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2011年の論文

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2011年論文

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Molecular Diagnosis of Congenital Adrenal Hyperplasia in Iran: Focusing on CYP21A2 Gene.

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Molecular Diagnosis of Congenital Adrenal Hyperplasia in Iran: Focusing on CYP21A2 Gene.

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Molecular Diagnosis of Congenital Adrenal Hyperplasia in Iran: Focusing on CYP21A2 Gene.

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Molecular Diagnosis of Congenital Adrenal Hyperplasia in Iran: Focusing on CYP21A2 Gene.

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Molecular Diagnosis of Congenital Adrenal Hyperplasia in Iran: Focusing on CYP21A2 Gene.

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Molecular Diagnosis of Congenital Adrenal Hyperplasia in Iran: Focusing on CYP21A2 Gene.

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P1476

Molecular Diagnosis of Congenital Adrenal Hyperplasia in Iran: Focusing on CYP21A2 Gene.

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P2093

Ali Rabbani

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Bahareh Rabbani

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Mohammad-Taghi Akbari

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Mohammad-Taghi Haghi Ashtiani

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Nejat Mahdieh

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P2860

Tenascin-X: a novel extracellular matrix protein encoded by the human XB gene overlapping P450c21B

The genetic and functional basis of isolated 17,20-lyase deficiency

Nonclassic congenital lipoid adrenal hyperplasia: a new disorder of the steroidogenic acute regulatory protein with very late presentation and normal male genitalia

Role of steroidogenic acute regulatory protein in adrenal and gonadal steroidogenesis

Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome

Statistical study of 35delG mutation of GJB2 gene: a meta-analysis of carrier frequency.

Direct molecular diagnosis of CYP21 mutations in congenital adrenal hyperplasia

Functional consequences of seven novel mutations in the CYP11B1 gene: four mutations associated with nonclassic and three mutations causing classic 11{beta}-hydroxylase deficiency.

Modular variations of the human major histocompatibility complex class III genes for serine/threonine kinase RP, complement component C4, steroid 21-hydroxylase CYP21, and tenascin TNX (the RCCX module). A mechanism for gene deletions and disease as

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

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139-150

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birth defect

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3446151

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Molecular Diagnosis of Congenital Adrenal Hyperplasia in Iran: Focusing on CYP21A2 Gene.

about

P2860

P2860

Molecular Diagnosis of Congenital Adrenal Hyperplasia in Iran: Focusing on CYP21A2 Gene.

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P932