Adams–Oliver syndrome in siblings with central nervous system findings, epilepsy, and developmental delay: Refining the features of a severe autosomal recessive variant-Reference-Cited by-同舟云学术

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Adams–Oliver syndrome in siblings with central nervous system findings, epilepsy, and developmental delay: Refining the features of a severe autosomal recessive variant

Published:2008 Issue:4 Volume:146A Page:488-491
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

McGoey Robin R.,Lacassie Yves

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference14 articles.

1. HEREDITARY DEFORMITIES IN MAN

2. Polymicrogyria associated with scalp and limb defects: Variant of Adams-Oliver syndrome

3. Adams-Oliver syndrome: A case with juvenile chronic myelogenous leukemia and chylothorax

4. CONGENITAL DEFECT OF THE SCALP

5. Adams-Oliver syndrome: Autosomal recessive inheritance and new phenotypic-anthropometric findings

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1. A Child with a Congenital Aplasia of the Scalp: A Quiz;Acta Dermato-Venereologica;2024-06-17

2. A novel DLL4 mutation in Adams–Oliver syndrome with absence of the right pulmonary artery in newborn;American Journal of Medical Genetics Part A;2021-11-10

3. Terminal transverse limb defects;Birth Defects Research;2021-07-14

4. Terminal transverse limb defects with “nubbins”;Birth Defects Research;2021-07-08

5. A Newborn with Scalp Defect and Terminal Limbs Anomalies;Challenging Cases in Dermatology Volume 2;2019

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