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Volumn 39, Issue 10, 2002, Pages
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A rare case of a de novo dup(19q) associated with a mild phenotype.
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Author keywords
[No Author keywords available]
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Indexed keywords
CASE REPORT;
CHROMOSOME 19;
DEVELOPMENTAL DISORDER;
FEMALE;
GENE DUPLICATION;
GENETICS;
HUMAN;
LETTER;
PHENOTYPE;
PRESCHOOL CHILD;
CHILD, PRESCHOOL;
CHROMOSOMES, HUMAN, PAIR 19;
DEVELOPMENTAL DISABILITIES;
FEMALE;
GENE DUPLICATION;
HUMANS;
PHENOTYPE;
MLCS;
MLOWN;
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EID: 0036778421
PISSN: None
EISSN: 14686244
Source Type: Journal
DOI: 10.1136/jmg.39.10.e61 Document Type: Letter |
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Times cited : (17)
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References (0)
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