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Volumn 64, Issue 3, 1996, Pages 523-524
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Is the autosomal dominant Opitz GBBB syndrome part of the DiGeorge/velocardiofacial syndrome with deletions of chromosome area 22q11.2? [2]
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Author keywords
[No Author keywords available]
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Indexed keywords
AUTOSOMAL DOMINANT DISORDER;
CHROMOSOME 22Q;
CHROMOSOME DELETION;
DIGEORGE SYNDROME;
FLUORESCENCE IN SITU HYBRIDIZATION;
HUMAN;
HYPERTELORISM;
LETTER;
PRIORITY JOURNAL;
CHROMOSOME 22;
CHROMOSOME ABERRATION;
CHROMOSOME DISORDER;
CONGENITAL HEART MALFORMATION;
CRANIOFACIAL MALFORMATION;
FEMALE;
GENETICS;
MALE;
MULTIPLE MALFORMATION SYNDROME;
NOTE;
SYNDROME;
ABNORMALITIES, MULTIPLE;
CHROMOSOME ABERRATIONS;
CHROMOSOME DELETION;
CHROMOSOME DISORDERS;
CHROMOSOMES, HUMAN, PAIR 22;
CRANIOFACIAL ABNORMALITIES;
DIGEORGE SYNDROME;
FEMALE;
HEART DEFECTS, CONGENITAL;
HUMANS;
MALE;
SYNDROME;
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EID: 4243470351
PISSN: 01487299
EISSN: None
Source Type: Journal
DOI: 10.1002/ajmg.1320640303 Document Type: Letter |
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Times cited : (3)
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References (0)
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