Molecular and phenotypic analysis of the chromosome 22 microdeletion syndromes

Prog Clin Biol Res. 1993:384:207-24.

Authors

B S Emanuel¹, D Driscoll, E Goldmuntz, S Baldwin, J Biegel, E H Zackai, D McDonald-McGinn, B Sellinger, N Gorman, S Williams, et al.

Affiliation

¹ Department of Pediatrics, University of Pennsylvania, School of Medicine, Philadelphia 19104.

PMID: 8115404

No abstract available

Publication types

Research Support, U.S. Gov't, P.H.S.
Review

MeSH terms

Chromosome Deletion*
Chromosome Mapping
Chromosomes, Human, Pair 22*
Humans
Phenotype
Syndrome

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