Chromosome 22q11.2 deletion in a boy with Opitz (G/BBB) syndrome
- 29 March 1996
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics
- Vol. 62 (3), 274-275
- https://doi.org/10.1002/(sici)1096-8628(19960329)62:3<274::aid-ajmg13>3.0.co;2-h
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.Journal of Medical Genetics, 1993
- Opitz (BBB/G) syndrome: Oral manifestationsAmerican Journal of Medical Genetics, 1992
- The telecanthus-hypospadias syndrome.Journal of Medical Genetics, 1988
- Male to male transmission of the G syndromeClinical Genetics, 1983