A Novel 22q11.2 Microdeletion in DiGeorge Syndrome
- 1 February 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 64 (2) , 659-667
- https://doi.org/10.1086/302235
Abstract
No abstract availableThis publication has 30 references indexed in Scilit:
- Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndromeNature Genetics, 1997
- Molecular Definition of 22q11 Deletions in 151 Velo-Cardio-Facial Syndrome PatientsAmerican Journal of Human Genetics, 1997
- Family studies in chromosome 22q11 deletion: further demonstration of phenotypic heterogeneityClinical Dysmorphology, 1995
- Velo‐cardio‐facial syndrome and DiGeorge sequence with meningomyelocele and deletions of the 22q11 regionAmerican Journal of Medical Genetics, 1994
- The 1993–94 Généthon human genetic linkage mapNature Genetics, 1994
- Two simple procedures for releasing chromatin from routinely fixed cells for fluorescence in situ hybridizationCytogenetic and Genome Research, 1994
- CATCH 22.Journal of Medical Genetics, 1993
- Noonan's and DiGeorge syndromes with monosomy 22q11.Archives of Disease in Childhood, 1993
- The DiGeorge anomaly as a developmental field defectAmerican Journal of Medical Genetics, 1986
- The spectrum of the DiGeorge syndromeThe Journal of Pediatrics, 1979