No evidence for chromosomal microdeletions at the second DiGeorge syndrome locus on 10p near D10S585

Am J Med Genet. 1999 Apr 23;83(5):425-6. doi: 10.1002/(sici)1096-8628(19990423)83:5<425::aid-ajmg17>3.0.co;2-q.

Authors

O Bartsch, A Wagner, G K Hinkel, P Lichtner, J Murken, S Schuffenhauer

PMID: 10232757
DOI: 10.1002/(sici)1096-8628(19990423)83:5<425::aid-ajmg17>3.0.co;2-q

No abstract available

Publication types

Letter
Research Support, Non-U.S. Gov't

MeSH terms

Child
Child, Preschool
Chromosome Deletion*
Chromosomes, Human, Pair 10*
DiGeorge Syndrome / genetics*
Female
Humans
In Situ Hybridization, Fluorescence
Infant
Infant, Newborn
Karyotyping
Male