Novel X-chromosomal defect associated with abnormal ovarian function

Journal of Obstetrics and Gynaecology Research

Volumn 31, Issue 1, 2005, Pages 12-15

  Rao, Lakshmi ^a   Babu, Arvind ^a   Padmalatha, Venkata ^a   Kanakavalli, Murthy ^a   Deenadayal, Mamata ^b   Singh, Lalji ^a  

^a CENTRE FOR CELLULAR AND MOLECULAR BIOLOGY   (India)

^b Infertility Institute and Research Centre   (India)

Author keywords

Cytogenetic analysis; Fluorescence in situ hybridization analysis; Premature ovarian failure; X chromosome defect

Indexed keywords

ADULT; ARTICLE; AUTOIMMUNE DISEASE; CASE REPORT; CHROMOSOME DELETION X; CLINICAL EXAMINATION; CLINICAL FEATURE; CYTOGENETICS; DISEASE ASSOCIATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC ANALYSIS; GENETIC DISORDER; HUMAN; KARYOTYPING; OVARY INSUFFICIENCY; PREMATURE OVARIAN FAILURE; PRIMARY AMENORRHEA; TURNER SYNDROME; X CHROMOSOME ABERRATION;

ADULT; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, X; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; OVARIAN FAILURE, PREMATURE;

EID: 14944355907     PISSN: 13418076     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1447-0756.2005.00235.x     Document Type: Article

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