Autosomal dominant “Opitz” GBBB syndrome due to a 22q11.2 deletion
- 23 August 1996
- journal article
- letter
- Published by Wiley in American Journal of Medical Genetics
- Vol. 64 (3) , 525-526
- https://doi.org/10.1002/ajmg.1320640304
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Is the autosomal dominant Opitz GBBB syndrome part of the DiGeorge/velocardiofacial syndrome with deletions of chromosome area 22q11.2?American Journal of Medical Genetics, 1996
- Chromosome 22q11.2 deletion in a boy with Opitz (G/BBB) syndromeAmerican Journal of Medical Genetics, 1996
- Interstitial 22q11 microdeletion excluding the ADU breakpoint in a patient with DiGeorge syndromeHuman Molecular Genetics, 1995
- Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2Nature Genetics, 1995
- Autosomal dominant “Opitz” GBBB syndrome due to a 22q11. 2 deletionAmerican Journal of Medical Genetics, 1995
- G syndrome: An unusual familyAmerican Journal of Medical Genetics, 1988
- G syndrome (hypertelorism with esophageal abnormality and hypospadias, or hypospadias‐dysphagia, or “Opitz‐Frias” or “opitz‐G” syndrome)—perspective in 1987 and bibliographyAmerican Journal of Medical Genetics, 1987
- TheGsyndrome-additional observationsAmerican Journal of Medical Genetics, 1980