Characterization of 10p deletions suggests two nonoverlapping regions contribute to the DiGeorge syndrome phenotype - PubMed (original) (raw)
- PMID: 9463325
- PMCID: PMC1376894
- DOI: 10.1086/301718
Characterization of 10p deletions suggests two nonoverlapping regions contribute to the DiGeorge syndrome phenotype
S Gottlieb et al. Am J Hum Genet. 1998 Feb.
No abstract available
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