Prenatal diagnosis of Lesch-Nyhan syndrome: Experience with three fetuses at risk-Reference-Cited by-同舟云学术

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Prenatal diagnosis of Lesch-Nyhan syndrome: Experience with three fetuses at risk

Published:1989-09 Issue:9 Volume:9 Page:657-661
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Zoref-Shani E.,Bromberg Y.,Goldman B.,Shaki R.,Barkai G.,Legum C.,Sperling O.

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference11 articles.

1. Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency: Activity in Normal, Mutant, and Heterozygote-Cultured Human Skin Fibroblasts

2. Studies on Hypoxanthine-Guanine Phosphoribosyltransferase in Fibroblasts from Patients with the Lesch-Nyhan Syndrome

3. A familial disorder of uric acid metabolism and central nervous system function

Cited by 5 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. Lesch-Nyhan Syndrome;Neurocutaneous Disorders Phakomatoses and Hamartoneoplastic Syndromes;2008

2. PRENATAL DIAGNOSIS BY ENZYME ANALYSIS IN 15 PREGNANCIES AT RISK FOR THE LESCH–NYHAN SYNDROME;Prenatal Diagnosis;1996-07

3. Lesch-Nyhan Syndrome in Two Brothers: Why Early Diagnosis is Essential;Clinical Pediatrics;1994-02

4. Jacobus de Voragine (1230-1298): First to Describe a Lesch-Nyhan Syndrome?;European Journal of Pediatric Surgery;1992-12

5. A catalogue of multiple congenital anomaly syndromes;Multiple Congenital Anomalies;1991

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