Is the autosomal dominant Opitz GBBB syndrome part of the DiGeorge/velocardiofacial syndrome with deletions of chromosome area 22q11.2?
- 23 August 1996
- journal article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 64 (3) , 523-524
- https://doi.org/10.1002/ajmg.1320640303
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- 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
- Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate geneNature Genetics, 1995
- Cloning of a balanced translocation breakpoint in the DiGeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinityHuman Molecular Genetics, 1995
- Submicroscopic deletions at 22q11.2: Variability of the clinical picture and delineation of a commonly deleted regionAmerican Journal of Medical Genetics, 1995
- Variable phenotypes in velocardiofacial syndrome with chromosomal deletionThe Journal of Pediatrics, 1993
- 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
- Contiguous gene syndromes: A component of recognizable syndromesThe Journal of Pediatrics, 1986