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letter . 1998 Feb;62(2):495–498. doi: 10.1086/301718
Characterization of 10p deletions suggests two nonoverlapping regions contribute to the DiGeorge syndrome phenotype.
S Gottlieb
, D A Driscoll
, H H Punnett
, B Sellinger
, B S Emanuel
, M L Budarf
S Gottlieb
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D A Driscoll
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H H Punnett
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B Sellinger
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B S Emanuel
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M L Budarf
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PMCID: PMC1376894 PMID: 9463325