Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus
- 9 May 1992
- journal article
- Published by Elsevier in The Lancet
- Vol. 339 (8802) , 1138-1139
- https://doi.org/10.1016/0140-6736(92)90734-k
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Isolation of anonymous DNA markers for human chromosome 22q11 from a flow-sorted library, and mapping using hybrids from patients with DiGeorge syndromeHuman Genetics, 1992
- DiGeorge syndrome with isolated aortic coarctation and isolated ventricular septal defect in three sibs with a 22q11 deletion of maternal origin.Heart, 1991
- Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndromeGenomics, 1991
- Localization of 27 DNA markers to the region of human chromosome 22q11-pter deleted in patients with the DiGeorge syndrome and duplicated in the der22 syndromeGenomics, 1990