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

Author:

Brunner H G,Winter R M

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference12 articles.

1. Oesophageal atresia in the south-west of England. J7 Med;David, T.J.; O'Caflaghan, S.E.;Genet,1975

2. Etiological study on isolated esophageal atresia;Szendrey, T.; Danyi, G.; Czeizel, A.;Hum Genet,1985

3. Family studies on congenital esophageal atresia with or without tracheoesophageal fistula;Chen, H.; Goei, G.S.; Hertzler, J.H.;Birth Defects,1979

4. Familial congenital esophageal atresia. Personal case report and review of the literature;M, Van Staey; de Bie S; MT, Matton; J, De Roose;Hum Genet,1984

5. Offspring of patients with tracheo-oesophageal fistula;Warren, J.; Evans, K.; Carter, C.O.;J Med Genet,1979

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