PRENATAL DIAGNOSIS OF CONGENITAL ADRENAL HYPERPLASIA (21-HYDROXYLASE DEFICIENCY) BY HLA TYPING
Authors:
- 1 May 1979
- journal article
- research article
- Published by Elsevier in The Lancet
- Vol. 313 (8126) , 1107-1108
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Genetic Mapping of the 21-Hydroxylase-Deficiency Gene within the HLA Linkage GroupNew England Journal of Medicine, 1978
- HLA AND CONGENITAL ADRENAL HYPERPLASIAThe Lancet, 1978
- Prenatal Diagnosis of Genetic DisordersScience, 1978
- Maternal and amniotic fluid 17α-hydroxyprogesterone levels during pregnancy: Diagnosis of congenital adrenal hyperplasia in uteroAmerican Journal of Obstetrics and Gynecology, 1978
- HLA AND CONGENITAL ADRENAL HYPERPLASIA LINKAGE CONFIRMEDThe Lancet, 1978
- CLOSE GENETIC LINKAGE BETWEEN HLA AND CONGENITAL ADRENAL HYPERPLASIA (21-HYDROXYLASE DEFICIENCY)The Lancet, 1977
- Microfilter Paper Method for 17α-Hydroxyprogesterone Radioimmunoassay: Its Application for Rapid Screening for Congenital Adrenal HyperplasiaThe Journal of Clinical Endocrinology & Metabolism, 1977
- Prenatal Diagnosis of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase DeficiencyPediatrics, 1977
- Elevated amniotic fluid concentration of 17 α-hydroxyprogesterone in congenital adrenal hyperplasiaThe Journal of Pediatrics, 1975