A case of 46,X,der(X)t(X;X)(q22.1;p11) Xq22.1→Xqter in a 12-year-old girl with premature ovarian failure

Gynecologic and Obstetric Investigation

Volumn 63, Issue 3, 2007, Pages 137-139

  Merhi, Z O ^a   Roberts, J L ^a   Awonuga, A O ^a  

^a MAIMONIDES MEDICAL CENTER   (United States)

Author keywords

Fluorescent in situ hybridization; Karyotype; Premature ovarian failure; Recombinant X chromosome

Indexed keywords

ARTICLE; C BANDING; CASE REPORT; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME XP; CHROMOSOME XQ; COMPARATIVE GENOMIC HYBRIDIZATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE LOCUS; GENETIC ANALYSIS; HORMONE SUBSTITUTION; HUMAN; KARYOTYPE; PHENOTYPE; PREMATURE OVARIAN FAILURE; PRIORITY JOURNAL; SCHOOL CHILD; X CHROMOSOME;

CHILD; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 22; CHROMOSOMES, HUMAN, X; FEMALE; GENE DELETION; GENE DUPLICATION; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; OVARIAN FAILURE, PREMATURE;

EID: 34047178483     PISSN: 03787346     EISSN: None     Source Type: Journal    
DOI: 10.1159/000096436     Document Type: Article

References (10)

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