Familial Klippel–Feil anomaly and t(5;8)(q35.1;p21.1) translocation
- 14 April 2006
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics Part A
- Vol. 140A (9), 1013-1015
- https://doi.org/10.1002/ajmg.a.31198
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Klippel-Feil SyndromeClinical Orthopaedics & Related Research, 2004
- De novo inv(2)(p12q34) associated with Klippel-Feil anomaly and hypodontiaEuropean Journal of Pediatrics, 2003
- De novo apparently balanced reciprocal translocation between 5q1l.2 and 17q23 associated with Klippel‐Feil anomaly and type A1 brachydactylyAmerican Journal of Medical Genetics, 1995
- THE KLIPPEL-FEIL SYNDROME: GENETIC AND CLINICAL REEVALUATION OF CERVICAL FUSIONMedicine, 1967