Molecular and cytogenetic study on 18 cases of amenorrhea: The use of fluorescence in situ hybridization and high resolution-comparative genomic hybridization

Chinese Journal of Medical Genetics

Volumn 24, Issue 3, 2007, Pages 256-260

  Kong, Hui ^a   Ge, Yun Sheng ^a   Wu, Qiong ^a   Wu, Hui Nan ^a   Zhou, Dong Xing ^a   Shen, Yan Yan ^a   Zheng, Yan Ling ^a   Cai, Mei Jiao ^a   Li, Jian ^a   Huang, Xin Li ^b  

^a Xiamen Maternity and Child Health Care Hospital   (China)

^b BOSTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Chromosomal abnormality; Fluorescence in situ hybridization; High resolution comparative hybridization; Primary amenorrhea

Indexed keywords

AMENORRHEA; ARTICLE; CHROMOSOME ANALYSIS; CHROMOSOME TRANSLOCATION; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GYNECOLOGICAL EXAMINATION; HUMAN; ISOCHROMOSOME X; KARYOTYPE 45,X; KARYOTYPE 46,XX; KARYOTYPE 46,XY; MOLECULAR GENETICS; PARTIAL MONOSOMY; TURNER SYNDROME;

ADOLESCENT; ADULT; AMENORRHEA; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN; COMPARATIVE GENOMIC HYBRIDIZATION; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING;

EID: 34250872775     PISSN: 10039406     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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