Interstitial deletions of chromosome 6q: Genotype-phenotype correlation utilizing array CGH

Clinical Genetics

Volumn 71, Issue 3, 2007, Pages 260-266

  Klein, O D ^a   Cotter, P D ^a,b   Moore, M W ^c   Zanko, A ^a   Gilats, M ^a   Epstein, C J ^a   Conte, F ^a   Rauen, Katherine A ^a,d  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b CHILDREN S HOSPITAL OAKLAND   (United States)

^c Combimatrix Molecular Diagnostics ^*  (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ANEUPLOIDY; ARTICLE; BRAIN DEVELOPMENT; CASE REPORT; CHILD; CHROMOSOME 6; CHROMOSOME 6Q; CHROMOSOME ANALYSIS; CHROMOSOME ARM; CHROMOSOME REARRANGEMENT; COMPARATIVE GENOMIC HYBRIDIZATION; CRANIOFACIAL DEVELOPMENT; CRANIOFACIAL MALFORMATION; DEVELOPMENTAL DISORDER; DIABETES INSIPIDUS; EYE DISEASE; GENE FUNCTION; GENE LOCATION; GENOTYPE PHENOTYPE CORRELATION; HUMAN; INTERSTITIAL CHROMOSOME DELETION; KARYOTYPE 46,XY; KARYOTYPING; MALE; MONOSOMY; PHENOTYPIC VARIATION; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; ADOLESCENT; ANEUPLOIDY; CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 6; CYTOGENETIC ANALYSIS; DEVELOPMENTAL DISABILITIES; FEMALE; GENOTYPE; HUMANS; MALE; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PHENOTYPE;

EID: 33847255395     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2007.00757.x     Document Type: Article

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