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Volumn 103, Issue 3, 2001, Pages 231-234

Direct duplication of 8p21.3→p23.1: A cytogenetic anomaly associated with developmental delay without consistent clinical features

(5) Fan, Yao Shan a Siu, Victoria M a Jung, Jack H a Farrell, S A b Côté, Gilbert B c

a LONDON HEALTH SCIENCES CENTRE (Canada)

b CREDIT VALLEY HOSPITAL (Canada)

c SUDBURY REGIONAL HOSPITAL (Canada)

Author keywords

Chromosome 8; Chromosome abnormality; Developmental delay; Direct duplication of 8p; FISH; Mental retardation

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 8P; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME DUPLICATION; CHROMOSOME HIGH RESOLUTION BANDING ANALYSIS; CHROMOSOME MOSAICISM; CLINICAL FEATURE; CYTOGENETICS; DEVELOPMENTAL DISORDER; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; INFANT; MENTAL RETARDATION MALFORMATION SYNDROME; PHENOTYPE; PRIORITY JOURNAL;

CHROMOSOME ABERRATIONS; CHROMOSOME PAINTING; CHROMOSOMES, HUMAN, PAIR 8; DEVELOPMENTAL DISABILITIES; FEMALE; GENE DUPLICATION; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; KARYOTYPING; MALE; MENTAL RETARDATION; MOSAICISM; PHENOTYPE; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 0035888107 PISSN: 01487299 EISSN: None Source Type: Journal
DOI: 10.1002/ajmg.1534 Document Type: Article

Times cited : (14)

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