21-hydroxylase deficiency families with HLA identical affected and unaffected sibs.-Reference-Cited by-同舟云学术

21-hydroxylase deficiency families with HLA identical affected and unaffected sibs.

Published:1989-01-01 Issue:1 Volume:26 Page:10-17
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Sinnott P J,Dyer P A,Price D A,Harris R,Strachan T

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference30 articles.

1. Congenital adrenal hyperplasia. Parts 1 and 2;White, P.C.; New, M.I.; Dupont, B.;N Engl J Med,1987

2. Molecular and clinical advances in congenital adrenal hyperplasia;Miller, W.L.; Levine, L.S.;J Pediatr,1987

3. Close genetic linkage between HLA and congenital adrenal hyperplasia (21-hydroxylase deficiency);Dupont, B.; Oberfield, S.E.; Smithwick, E.M.; Lee, T.D.; Levine, L.S.;Lancet,1977

4. HLA and congenital adrenal hyperplasia linkage confirmed;Price, D.A.; Klouda, P.T.; Harris, R.;Lancet,1978

5. Varying expression for salt-losing in related patients with congenital adrenal hyperplasia;Rosenbloom, A.L.; Smith, D.W.;Pediatrics,1966

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2. The Adrenal Cortex and Its Disorders;Pediatric Endocrinology;2008

3. Mutation distribution and CYP21/C4 locus variability in Brazilian families with the classical form of the 21-hydroxylase deficiency;Acta Paediatrica;2007-01-02

4. The Implication of De Novo 21-Hydroxylase Mutation in Clinical and Prenatal Molecular Diagnoses;Genetic Testing;2005-06

5. Mutation distribution and CYP21/C4 locus variability in Brazilian families with the classical form of the 21-hydroxylase deficiency;ACTA PAEDIATR;1999