The Spectrum of Mutations in TBX3: Genotype/Phenotype Relationship in Ulnar-Mammary Syndrome
- 1 June 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 64 (6), 1550-1562
- https://doi.org/10.1086/302417
Abstract
No abstract availableKeywords
This publication has 44 references indexed in Scilit:
- Cloning, Mapping, and Expression Analysis ofTBX15,a New Member of the T-Box Gene FamilyGenomics, 1998
- Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndromeNature Genetics, 1997
- Newly Identified Paralogous Groups on Mouse Chromosomes 5 and 11 Reveal the Age of a T-Box Cluster DuplicationGenomics, 1997
- Mutations in human cause limb and cardiac malformation in Holt-Oram syndromeNature Genetics, 1997
- Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene familyNature Genetics, 1997
- Retinoic Acid Induces Three Newly Cloned HOXA1 Transcripts in MCF7 Breast Cancer CellsBiochemical and Biophysical Research Communications, 1995
- Mesoderm formation in response to Brachyury requires FGF signallingCurrent Biology, 1995
- Possible relationship between ulnar-mammary syndrome and split hand with aplasia of the ulna syndromeAmerican Journal of Medical Genetics, 1992
- Basic local alignment search toolJournal of Molecular Biology, 1990
- The ulnar‐mammary syndrome: an autosomal dominant pleiotropic geneClinical Genetics, 1987