Syndromic Ectrodactyly with Severe Limb, Ectodermal, Urogenital, and Palatal Defects Maps to Chromosome 19
- 1 January 1998
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 62 (1) , 130-135
- https://doi.org/10.1086/301687
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- The lobster claw defect with ectodermal defects, cleft lip-palate, tear duct anomaly and renal anomaliesClinical Genetics, 2008
- Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndromeNature Genetics, 1997
- Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb developmentHuman Molecular Genetics, 1996
- A comprehensive genetic map of the human genome based on 5,264 microsatellitesNature, 1996
- Twenty-four cases of the EEC syndrome: clinical presentation and management.Journal of Medical Genetics, 1995
- Vertebrate limb developmentCurrent Opinion in Genetics & Development, 1995
- Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactylyHuman Molecular Genetics, 1994
- Transforming growth factor‐β and bone morphogenetic protein‐2 act by distinct mechanisms to promote chick limb cartilage differentiation in vitroDevelopmental Dynamics, 1994
- Rapid induction and clearance of TGFβ1 is an early response to wounding in the mouse embryoDevelopmental Genetics, 1993
- Possible relationship between ulnar-mammary syndrome and split hand with aplasia of the ulna syndromeAmerican Journal of Medical Genetics, 1992