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Volumn 76, Issue 1, 1997, Pages 79-80
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Chromosome 22q11 microdeletion and isolated conotruncal heart defects [2]
a a a a |
Author keywords
[No Author keywords available]
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Indexed keywords
CHILD;
CHROMOSOME 22Q;
CONGENITAL HEART DISEASE;
HUMAN;
IN SITU HYBRIDIZATION;
LETTER;
PHENOTYPE;
PRIORITY JOURNAL;
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EID: 0031037717
PISSN: 00039888
EISSN: 14682044
Source Type: Journal
DOI: 10.1136/adc.76.1.79a Document Type: Letter |
Times cited : (16)
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References (6)
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