First Trimester Prenatal Diagnosis of Smith-Lemli-Opitz Syndrome(7-Dehydrocholesterol Reductase Deficiency)-Reference-Cited by-同舟云学术

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First Trimester Prenatal Diagnosis of Smith-Lemli-Opitz Syndrome(7-Dehydrocholesterol Reductase Deficiency)

Published:1996-05 Issue:5 Volume:39 Page:816-819
ISSN:0031-3998
Container-title:Pediatric Research
language:
Short-container-title:Pediatr Res

Author:

Mills Kevin,Mandel Hanna,Montemagno Rodolfo,Soothill Peter,Gershoni-Baruch R,Clayton Peter T

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Reference13 articles.

1. A newly recognized syndromeof multiple congenital anomalies

2. Smith-Lemli-Opitz syndrome-type II: Multiple congenital anomalies with male pseudohermaphroditism and frequent early lethality

3. Smith-Lemli-Opitz (RSH) syndrome bibliography

4. Possible abnormalities of steroid secretion in children with Smith-Lemli-Opitz syndrome and their parents

5. Defective Cholesterol Biosynthesis Associated with the Smith-Lemli-Opitz Syndrome

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3. Smith‐Lemli‐Opitz syndrome — Fetal phenotypes with special reference to the syndrome‐specific internal malformation pattern;Birth Defects Research;2019-12-16

4. Smith–Lemli–Opitz Mutations in Unexplained Stillbirths;American Journal of Perinatology;2018-02-12

5. Mevalonate Cascade and Neurodevelopmental and Neurodegenerative Diseases: Future Targets for Therapeutic Application;Current Molecular Pharmacology;2017-03-01

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