Congenital adrenal hyperplasia in monozygotic twins with variable clinical manifestations-Reference-Cited by-同舟云学术

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Congenital adrenal hyperplasia in monozygotic twins with variable clinical manifestations

Published:1989-09 Issue:3 Volume:34 Page:231-234
ISSN:0021-5074
Container-title:Japanese journal of human genetics
language:en
Short-container-title:Jap J Human Genet

Author:

Kanjilal Debasis,Verma Ram S.,Glass Leonard,Babu Arvind,Ramazanoglu Fatih,Popescu Serpouhi

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical)

Link

http://www.nature.com/articles/jhg198920.pdf

Reference8 articles.

1. Gala, O.M., Rudd, B.T. and Drayer, N.M. 1969. Evaluation of deficiency of 21-hydroxylation in patients with congenital adrenal hyperplasia.Arch. Dis. Child. 43: 410–414.

2. McKusick, V.A. 1987.Mendelian Inheritance in Man, The John Hopkins Press, Baltimore.

3. Miller, W.L. and Levine, L.S. 1987. Molecular and clinical advances in congenital hyperplasia.J. Pediatr. 111: 1–17.

4. Murtaza, L., Sibert, J.R., Hughes, I. and Balfour, I.C. 1980. Congenital adrenal hyperplasia—a clinical and genetic survey: are we detecting male salt losers?Arch. Dis. Child. 55: 662.

5. New, M.I., Dupont, B., Pollack, M.S. and Levine, L.S. 1981. The biochemical basis for genotyping 21-hydroxylase deficiency.Hum. Genet. 58: 123–127.

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Twins and Twinning;Emery and Rimoin's Principles and Practice of Medical Genetics;2013

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