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Volumn 42, Issue 2, 1999, Pages 95-100
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Probing the human genome in search for a new 3q syndrome
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Author keywords
Chromosome 3; FISH technique; Trisomy 3q syndrome
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Indexed keywords
ARTICLE;
BEHAVIOR DISORDER;
CASE REPORT;
CHROMOSOME 10P;
CHROMOSOME 15Q;
CHROMOSOME 16P;
CHROMOSOME 18Q;
CHROMOSOME 20Q;
CHROMOSOME 2P;
CHROMOSOME 3Q;
CHROMOSOME 4;
CHROMOSOME 6P;
CHROMOSOME 8P;
CHROMOSOME ABERRATION;
CHROMOSOME ANALYSIS;
CLINICAL FEATURE;
EYEBROW;
FACIES;
FLUORESCENCE IN SITU HYBRIDIZATION;
FRONTAL BOSSING;
GENOME;
HUMAN;
INGUINAL HERNIA;
MALE;
NOSE;
PARTIAL TRISOMY;
PROMINENT EAR;
PSYCHOMOTOR DISORDER;
SCHOOL CHILD;
SYNDROME;
CHILD;
CHROMOSOMES, HUMAN, PAIR 3;
CHROMOSOMES, HUMAN, PAIR 4;
DNA PROBES;
GENOME, HUMAN;
HUMANS;
IN SITU HYBRIDIZATION, FLUORESCENCE;
KARYOTYPING;
MALE;
SYNDROME;
TRISOMY;
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EID: 0032842533
PISSN: 00033995
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
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Times cited : (6)
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References (28)
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