Unrelated patients with a rearrangement of chromosome 2 causing duplication of 2p23 and deletion of 2q37

American Journal of Medical Genetics

Volumn 134 A, Issue 3, 2005, Pages 299-304

  Armstrong, Linlea ^a,d   Allanson, Judith E ^a   Weaver, David D ^b   Bevan, Carole J ^a   Hobart, Holly H ^a,b,c  

^a CHILDREN S HOSPITAL OF EASTERN ONTARIO   (Canada)

^b INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF NEVADA SCHOOL OF MEDICINE   (United States)

^d UNIVERSITY OF BRITISH COLUMBIA   (Canada)

Author keywords

Autistic; Chromosome 2; Partial monosomy; Partial trisomy; Terminal deletion 2q; Terminal duplication 2p

Indexed keywords

ADOLESCENT; ARTICLE; AUTISM; CASE REPORT; CHROMOSOME 2; CHROMOSOME 2P; CHROMOSOME 2Q; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME REARRANGEMENT; CLINICAL FEATURE; DEVELOPMENTAL DISORDER; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; FRONTAL BOSSING; GENETIC COUNSELING; HUMAN; INFANT; LOW SET EAR; MALE; MENTAL DEFICIENCY; MYCN GENE; NIPPLE MALFORMATION; ONCOGENE C MYB; PARTIAL MONOSOMY; PARTIAL TRISOMY; PERICENTRIC CHROMOSOME INVERSION; PRIORITY JOURNAL; SKIN DEFECT;

CHILD; CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 2; FEMALE; GENE DUPLICATION; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; INVERSION, CHROMOSOME; KARYOTYPING; MALE;

EID: 16344368873     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30502     Document Type: Article

References (13)

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