CATCH 22.
Open Access
- 1 October 1993
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 30 (10) , 801-802
- https://doi.org/10.1136/jmg.30.10.801
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.Journal of Medical Genetics, 1993
- Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.Journal of Medical Genetics, 1993
- DiGeorge syndrome: part of CATCH 22.Journal of Medical Genetics, 1993
- DiGeorge syndrome: an historical review of clinical and cytogenetic features.Journal of Medical Genetics, 1993
- Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects.Journal of Medical Genetics, 1993
- Velocardiofacial syndrome in a mother and daughter: variability of the clinical phenotype.Journal of Medical Genetics, 1993
- Isolation of a new marker and conserved sequences close to the DiGeorge syndrome marker HP500 (D22S134).Journal of Medical Genetics, 1993
- Molecular cytogenetics: toward dissection of the contiguous gene syndromes.1988
- Contiguous gene syndromes: A component of recognizable syndromesThe Journal of Pediatrics, 1986
- A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome.1978