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Volumn 64, Issue 3, 1996, Pages 525-526
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Autosomal dominant 'Opitz' GBBB syndrome due to a 22q11.2 deletion [3]
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Author keywords
[No Author keywords available]
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Indexed keywords
AUTOSOMAL DOMINANT DISORDER;
CHROMOSOME 22Q;
CHROMOSOME DELETION;
ESOPHAGUS MOTILITY;
HUMAN;
LETTER;
LUNG MALFORMATION;
MENTAL DEFICIENCY;
PRIORITY JOURNAL;
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EID: 0029833528
PISSN: 01487299
EISSN: None
Source Type: Journal
DOI: 10.1002/ajmg.1320640304 Document Type: Letter |
Times cited : (17)
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References (0)
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