EXTENDED MHC HAPLOTYPES IN 21-HYDROXYLASE-DEFICIENCY CONGENITAL ADRENAL HYPERPLASIA: SHARED GENOTYPES IN UNRELATED PATIENTS-Reference-Cited by-同舟云学术

EXTENDED MHC HAPLOTYPES IN 21-HYDROXYLASE-DEFICIENCY CONGENITAL ADRENAL HYPERPLASIA: SHARED GENOTYPES IN UNRELATED PATIENTS

Published:1983-01 Issue:8317 Volume:321 Page:152-156
ISSN:0140-6736
Container-title:The Lancet
language:en
Short-container-title:The Lancet

Author:

Fleischnick E,Raum D,Alosco S.M,Gerald P.S,Yunis E.J,Awdeh Z.L,Granados J,Crigler J.F,Giles C.M,Alper C.A

Publisher

Elsevier BV

Subject

General Medicine

Reference38 articles.

1. Congenital adrenal hyperplasia and related conditions;Bongiovanni,1978

2. Partial 11- and 21-hydroxylase deficiencies in hirsute women;Newmark;Am J Obstet Gynecol,1977

3. An attenuated form of congenital virilizing adrenal hyperplasia;Rosenwaks;J Clin Endocrinol Metab,1979

4. Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasia;Levine;J Clin Endocrinol Metab,1980

5. HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiency;Pollack;Am J Hum Genet,1981

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