Pitfalls of Prenatal Diagnosis of 21‐Hydroxylase Deficiency Congenital Adrenal Hyperplasiaa
- 1 November 1985
- journal article
- Published by Wiley in Annals of the New York Academy of Sciences
- Vol. 458 (1) , 111-129
- https://doi.org/10.1111/j.1749-6632.1985.tb14597.x
Abstract
No abstract availableThis publication has 23 references indexed in Scilit:
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- Prenatal diagnosis of congenital adrenal hyperplasia (21‐OH deficiency type) by HLA typingPrenatal Diagnosis, 1981
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- ANTENATAL DIAGNOSIS OF CONGENITAL ADRENAL HYPERPLASIAThe Lancet, 1979
- PRENATAL DIAGNOSIS OF CONGENITAL ADRENAL HYPERPLASIA (21-HYDROXYLASE DEFICIENCY) BY HLA TYPINGThe Lancet, 1979
- No Linkage between HLA and Congenital Adrenal Hyperplasia Due to 11-β-Hydroxylase DeficiencyNew England Journal of Medicine, 1979
- Prenatal diagnosis of congenital adrenal hyperplasiaAmerican Journal of Medical Genetics, 1979
- Genetic Mapping of the 21-Hydroxylase-Deficiency Gene within the HLA Linkage GroupNew England Journal of Medicine, 1978
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