Novel HOXA13 Mutations and the Phenotypic Spectrum of Hand-Foot-Genital Syndrome
- 1 July 2000
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 67 (1), 197-202
- https://doi.org/10.1086/302961
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Mutation of HOXA13 in hand-foot-genital syndromeNature Genetics, 1997
- Altered Growth and Branching Patterns in Synpolydactyly Caused by Mutations in HOXD13Science, 1996
- The hand‐foot‐genital syndrome: on the variable expression in affected malesClinical Genetics, 1993
- Update on a family with hand–foot–genital syndrome: Hypospadias and urinary tract abnormalities in two boys from the fourth generationAmerican Journal of Medical Genetics, 1992
- Crystal structure of a MATα2 homeodomain-operator complex suggests a general model for homeodomain-DNA interactionsCell, 1991
- Hand-foot-genital syndrome: the importance of hallux varusPediatric Radiology, 1990
- Acral‐genital anomalies combined with ear anomaliesAmerican Journal of Medical Genetics, 1989
- Urinary tract abnormalities in hand‐foot‐ genital syndromeAmerican Journal of Medical Genetics, 1989
- The Hand‐Foot‐Genital (Hand‐Foot‐Uterus) syndrome: Family report and updateAmerican Journal of Medical Genetics, 1988
- The hand-foot-uterus syndrome: A new hereditary disorder characterized by hand and foot dysplasia, dermatoglyphic abnormalities, and partial duplication of the female genital tractThe Journal of Pediatrics, 1970