A Locus for Brachydactyly Type A-1 Maps to Chromosome 2q35-q36
- 1 March 2000
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 66 (3) , 892-903
- https://doi.org/10.1086/302806
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- HoxGene Expression in Limbs: Colinearity by Opposite Regulatory ControlsDevelopmental Biology, 1999
- A boy with severe manifestations of type A1 brachydactylyClinical Dysmorphology, 1998
- Mutations in CDMP1 cause autosomal dominant brachydactyly type CNature Genetics, 1997
- Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tractProceedings of the National Academy of Sciences, 1997
- Altered Growth and Branching Patterns in Synpolydactyly Caused by Mutations in HOXD13Science, 1996
- A comprehensive genetic map of the human genome based on 5,264 microsatellitesNature, 1996
- The mutational spectrum in Waardenburg syndromeHuman Molecular Genetics, 1995
- A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage mapsHuman Molecular Genetics, 1995
- Hoxa-13 and Hoxd-13 play a crucial role in the patterning of the limb autopodDevelopment, 1995
- Mutations of the Gs alpha-subunit gene in Albright hereditary osteodystrophy detected by denaturing gradient gel electrophoresis.Proceedings of the National Academy of Sciences, 1990