Genomic analysis using high-resolution single-nucleotide polymorphism arrays reveals novel microdeletions associated with premature ovarian failure

Fertility and Sterility

Volumn 95, Issue 5, 2011, Pages 1595-1600

  McGuire, Megan M ^a   Bowden, Wayne ^b   Engel, Natalie J ^a   Ahn, Hyo Won ^a   Kovanci, Ertug ^b   Rajkovic, Aleksandar ^a  

^a UNIVERSITY OF PITTSBURGH   (United States)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

array CGH; chromosomal microarray; CNV; copy number; microdeletion and microduplication; POF; POI; Premature ovarian failure; SNP microarray

Indexed keywords

ADULT; ARTICLE; AUTOSOME; CASE CONTROL STUDY; CHROMOSOME 10P; CHROMOSOME 10Q; CHROMOSOME 15Q; CHROMOSOME 18Q; CHROMOSOME 8Q; CONTROLLED STUDY; COPY NUMBER VARIATION; DNA DETERMINATION; FEMALE; GENETIC ASSOCIATION; HUMAN; MAJOR CLINICAL STUDY; PREMATURE OVARIAN FAILURE; PRIMARY AMENORRHEA; PRIORITY JOURNAL; SECONDARY AMENORRHEA; SINGLE NUCLEOTIDE POLYMORPHISM; X CHROMOSOME;

ADULT; CASE-CONTROL STUDIES; CHROMOSOME DELETION; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOME, HUMAN; GENOME-WIDE ASSOCIATION STUDY; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PILOT PROJECTS; POLYMORPHISM, SINGLE NUCLEOTIDE; PRIMARY OVARIAN INSUFFICIENCY; YOUNG ADULT;

EID: 79952988259     PISSN: 00150282     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.fertnstert.2010.12.052     Document Type: Article

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