De novo 46,XX, dir dup (11)(q13.3 → q14.2) in a patient with mental retardation, congenital cardiopathy and thrombopenia

Clinical Genetics

Volumn 49, Issue 4, 1996, Pages 206-210

  Legius, E ^a   Wlodarska, I ^a   Selleri, L ^b   Evans, G A ^c   Wu, R ^a   Smet, G ^d   Fryns, J P ^a  

^a UNIVERSITY HOSPITALS LEUVEN   (Belgium)

^b STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF TEXAS AT DALLAS   (United States)

^d Internal Medicine   (Belgium)

Author keywords

Chromosome 11; FISH; Fluorescence in situ hybridization; Partial trisomy 11q; Tandem duplication

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 11Q; CHROMOSOME ANALYSIS; CHROMOSOME BANDING PATTERN; CHROMOSOME DUPLICATION; CHROMOSOME TRANSLOCATION 11; CONGENITAL HEART DISEASE; FACE DYSMORPHIA; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; KARYOTYPE 46,XX; LYMPHOCYTE; MENTAL DEFICIENCY; PARTIAL MONOSOMY; PARTIAL TRISOMY; PRIORITY JOURNAL; THROMBOCYTOPENIA;

EID: 0029989053     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1996.tb03288.x     Document Type: Article

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