Literature DB >> 631836

An unusual microcephaly.

M Feingold.   

Abstract

Mesh：

Year:  1978        PMID： 631836     DOI： 10.1080/21548331.1978.11707275

Source DB:  PubMed          Journal:  Hosp Pract        ISSN： 0018-5809


× No keyword cloud information.
  1 in total

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

Authors:  H G Brunner; R M Winter
Journal:  J Med Genet       Date:  1991-06       Impact factor: 6.318
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.