Distinctive autosomal or X-linked dominant syndrome of microcephaly, mild developmental delay, short stature, and distinctive face-Reference-Cited by-同舟云学术

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Distinctive autosomal or X-linked dominant syndrome of microcephaly, mild developmental delay, short stature, and distinctive face

Published:1993-11-01 Issue:6 Volume:47 Page:917-920
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Winter R. M.

Publisher

Wiley

Subject

Genetics (clinical)

Reference22 articles.

1. A syndrome of microcephaly, eye anomalies, short stature, and mental deficiency

2. Autosomal dominant microcephaly with mental retardation

3. Autosomal dominant inheritance of abnormalities of the hands and feet with short palpebral fissures, variable microcephaly with learning disability, and oesophageal/duodenal atresia.

4. Dominant inheritance of microcephaly with short stature

Cited by 3 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. REFERENCES (GAMUTS);Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007

2. Nonsyndromic Microcephaly: An Overview;Advances in Pediatrics;2005-01

3. Autosomal dominant microcephaly with normal intelligence, short palpebral fissures, and digital anomalies;American Journal of Medical Genetics;1997-08-08

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