Brachydactyly Type B: Clinical Description, Genetic Mapping to Chromosome 9q, and Evidence for a Shared Ancestral Mutation
- 1 February 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 64 (2) , 570-577
- https://doi.org/10.1086/302249
Abstract
No abstract availableKeywords
This publication has 40 references indexed in Scilit:
- Brachydactyly Type C Gene Maps to Human Chromosome 12q24Genomics, 1996
- A new syndrome of dwarfism, brachydactyly, nail dysplasia, and mental retardation in sibsAmerican Journal of Medical Genetics, 1990
- Sorsby syndrome: a report on further generations of the original family.Journal of Medical Genetics, 1988
- Autosomal dominant onychodystrophy and anonychia with type B brachydactyly and ectrodactylyClinical Genetics, 1986
- A new brachydactyly syndrome with similarities to Julia Bell types B and E.Journal of Medical Genetics, 1985
- Mackinder's hereditary brachydactyly: phenotypic, radiological, dermatoglyphic and genetic observations in an Ontario familyAnnals of Human Genetics, 1973
- BRACHYDACTYLY AND SYMBRACHYDACTYLYAnnals of Human Genetics, 1957
- Hereditary Phalangeal Agenesis showing dominant Mendelian CharacteristicsArchives of Disease in Childhood, 1947
- HEREDITARY BRACHYDACTYLIA AND ALLIED ABNORMALITIES IN THE RABBITThe Journal of Experimental Medicine, 1939
- Hereditary absence of phalanges through five generationsJournal of Genetics, 1916