A review of trisomy X (47,XXX)

Orphanet Journal of Rare Diseases

Volumn 5, Issue 1, 2010, Pages

  Tartaglia, Nicole R ^a,b   Howell, Susan ^a,b   Sutherland, Ashley ^a   Wilson, Rebecca ^b   Wilson, Lennie ^c  

^a Children's Hospital Colorado   (United States)

^b CHILDREN S HOSPITAL COLORADO   (United States)

^c MONTEFIORE MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ATTENTION DEFICIT DISORDER; CHROMOSOME ABERRATION; CLINICAL FEATURE; CLINODACTYLY; EPICANTHUS; GENOTYPE; HUMAN; KARYOTYPE; KIDNEY DISEASE; MOOD DISORDER; MUSCLE HYPOTONIA; PHENOTYPE; PREMATURE OVARIAN FAILURE; REVIEW; SEIZURE; TALL STATURE; TRISOMY; TRISOMY X; UROGENITAL TRACT DISEASE; X CHROMOSOME; FEMALE; GENETIC COUNSELING; GENETICS; KARYOTYPING; METHODOLOGY; PATHOLOGY; PATHOPHYSIOLOGY; PRENATAL DIAGNOSIS; SEX CHROMOSOME ABERRATION;

FEMALE; GENETIC COUNSELING; HUMANS; KARYOTYPING; PRENATAL DIAGNOSIS; SEX CHROMOSOME ABERRATIONS; TRISOMY;

EID: 77951946765     PISSN: None     EISSN: 17501172     Source Type: Journal    
DOI: 10.1186/1750-1172-5-8     Document Type: Review

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