Familial Syndromic Esophageal Atresia Maps to 2p23-p24
- 1 February 2000
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 66 (2) , 436-444
- https://doi.org/10.1086/302779
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- A Chromosomal Deletion Map of Human MalformationsAmerican Journal of Human Genetics, 1998
- Retinoic acid and retinoic acid receptors in craniofacial developmentSeminars in Cell & Developmental Biology, 1997
- The effects of Down syndrome and other chromosomal abnormalities on survival and management in oesophageal atresiaPediatric Surgery International, 1997
- Additional congenital anomalies in babies with gut atresia or stenosis: when to investigate, and which investigationPediatric Surgery International, 1997
- Mutations in the human Sonic Hedgehog gene cause holoprosencephalyNature Genetics, 1996
- A comprehensive genetic map of the human genome based on 5,264 microsatellitesNature, 1996
- Deletion of chromosome 2q24‐q31 causes characteristic digital anomalies: Case report and reviewAmerican Journal of Medical Genetics, 1995
- Familial occurrence of esophageal atresia with and without tracheoesophagel fistula:Report of two unusual kindredsAmerican Journal of Medical Genetics, 1991
- Autosomal dominant inheritance of abnormalities of the hands and feet with short palpebral fissures, variable microcephaly with learning disability, and oesophageal/duodenal atresia.Journal of Medical Genetics, 1991
- Oesophageal atresia in the South West of England.Journal of Medical Genetics, 1975