Molecular cytogenetic studies of Xq critical regions in premature ovarian failure patients

Human Reproduction

Volumn 21, Issue 9, 2006, Pages 2329-2334

  Portnoi M F ^a   Aboura, A ^b   Tachdjian, G ^b   Bouchard, P ^c   Dewailly, D ^d   Bourcigaux, N ^c   Frydman, R ^b   Reyss, Anne Céline ^d   Brisset, Sophie ^b   Christin Maitre, S ^c  

^a HÔPITAL SAINT ANTOINE   (France)

^b HÔPITAL ANTOINE BÉCLÈRE   (France)

^c SORBONNE UNIVERSITÉ   (France)

^d LILLE UNIVERSITY HOSPITAL   (France)

Author keywords

Deletion; Molecular cytogenetic; Premature ovarian failure; Translocation; X chromosome

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; BACTERIAL ARTIFICIAL CHROMOSOME; CHROMOSOME DELETION X; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION X; CHROMOSOME XQ; CONTROLLED STUDY; DNA MICROARRAY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPE 47,XXX; KARYOTYPING; MAJOR CLINICAL STUDY; METAPHASE CHROMOSOME; PATHOGENESIS; PHILADELPHIA 1 CHROMOSOME; PREMATURE OVARIAN FAILURE; ROBERTSONIAN CHROMOSOME TRANSLOCATION; SCHOOL CHILD;

BACTERIA (MICROORGANISMS); ROBERTSONIA;

EID: 33749576976     PISSN: 02681161     EISSN: 14602350     Source Type: Journal    
DOI: 10.1093/humrep/del174     Document Type: Article

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