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Volumn 95, Issue 3, 2000, Pages 296-
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Partial deletion of chromosome 12q is not usually associated with CFC syndrome [6]
a
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Author keywords
[No Author keywords available]
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Indexed keywords
ADOLESCENT;
CARDIO FACIO CUTANEOUS SYNDROME;
CHILD;
CHROMOSOME 12Q;
CHROMOSOME DELETION;
CLINICAL ARTICLE;
CONGENITAL HEART MALFORMATION;
CYTOGENETICS;
FACE MALFORMATION;
FEMALE;
FLUORESCENCE IN SITU HYBRIDIZATION;
GROWTH RETARDATION;
HUMAN;
HYDROCEPHALUS;
HYPERKERATOSIS;
INFANT;
KIDNEY MALFORMATION;
LETTER;
MACROCEPHALY;
MALE;
MENTAL DEFICIENCY;
PRIORITY JOURNAL;
ABNORMALITIES, MULTIPLE;
ADOLESCENT;
CARDIOVASCULAR ABNORMALITIES;
CHILD;
CHILD, PRESCHOOL;
CHROMOSOMES, HUMAN, PAIR 12;
CRANIOFACIAL ABNORMALITIES;
CYTOGENETIC ANALYSIS;
DIAGNOSTIC ERRORS;
FEMALE;
GENE DELETION;
HUMANS;
INFANT;
INFANT, NEWBORN;
MALE;
MENTAL RETARDATION;
PHENOTYPE;
SKIN ABNORMALITIES;
SYNDROME;
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EID: 0034722840
PISSN: 01487299
EISSN: None
Source Type: Journal
DOI: 10.1002/1096-8628(20001127)95:3<296::AID-AJMG24>3.0.CO;2-U Document Type: Letter |
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Times cited : (10)
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References (1)
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