Prenatal diagnosis of congenital adrenal hyperplasia-Reference-Cited by-同舟云学术

Prenatal diagnosis of congenital adrenal hyperplasia

Published:1979 Issue:2 Volume:4 Page:201-204
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Marcus E. S.,Holcombe J. H.,Tulchinsky D.,Rich R. R.,Riccardi V. M.,Karp Lawrence E.

Publisher

Wiley

Subject

Genetics (clinical)

Reference17 articles.

1. Maternal and amniotic fluid 17α-hydroxyprogesterone levels during pregnancy: Diagnosis of congenital adrenal hyperplasia in utero

2. Genetic Mapping of the 21-Hydroxylase-Deficiency Gene within the HLA Linkage Group

3. Radioimmunoassay of Plasma 17-Hydroxyprogesterone

4. Staff, Research Resources Branch, NIAID: NIH lymphocyte microcytotoxicity technique. NIAID Manual of Tissue Typing Techniques, Publication No. NIH 78-545. Washington, DC: US Department of Health Education and Welfare, 1976, pp 22-24.

Cited by 11 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. Technical Report: Congenital Adrenal Hyperplasia;Pediatrics;2000-12-01

2. Profiling Steroid Hormones in Amniotic Fluid of Midpregnancy by Routine Stable Isotope Dilution/Gas Chromatography-Mass Spectrometry: Reference Values and Concentrations in Fetuses at Risk for 21-Hydroxylase Deficiency;Journal of Clinical Endocrinology & Metabolism;1999-08-01

3. Profiling Steroid Hormones in Amniotic Fluid of Midpregnancy by Routine Stable Isotope Dilution/Gas Chromatography-Mass Spectrometry: Reference Values and Concentrations in Fetuses at Risk for 21-Hydroxylase Deficiency1;The Journal of Clinical Endocrinology & Metabolism;1999-08-01

4. Prenatal Detection of Congenital Adrenal Hyperplasia;Genetic Disorders and the Fetus;1986

5. Pitfalls in Prenatal Diagnosis of 21-Hydroxylase Deficiency by Amniotic Fluid Steroid Analysis? A Six Years Experience in 102 Pregnancies at Risk;Annals of the New York Academy of Sciences;1985-11