Identification of copy number variants in miscarriages from couples with idiopathic recurrent pregnancy loss | Zendy

Evica RajcanSeparovic | Zendy; Dan DiegoÁlvarez | Zendy; Wendy P. Robinson | Zendy; Christine Tyson | Zendy; Ying Qiao | Zendy; Chansonette Harvard | Zendy; Chris Fawcett | Zendy; Dagmar K. Kalousek | Zendy; Tom Philipp | Zendy; Martin J. Somerville | Zendy; Mary D. Stephenson | Zendy

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Identification of copy number variants in miscarriages from couples with idiopathic recurrent pregnancy loss

Author(s) -

Evica RajcanSeparovic,

Dan DiegoÁlvarez,

Wendy P. Robinson,

Christine Tyson,

Ying Qiao,

Chansonette Harvard,

Chris Fawcett,

Dagmar K. Kalousek,

Tom Philipp,

Martin J. Somerville,

Mary D. Stephenson

Publication year - 2010

Publication title -

human reproduction

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 2.446

H-Index - 226

eISSN - 1460-2350

pISSN - 0268-1161

DOI - 10.1093/humrep/deq202

Subject(s) - pregnancy , identification (biology) , obstetrics , medicine , copy number variation , gynecology , biology , genetics , genome , gene , botany

Recurrent pregnancy loss (RPL), defined as two or more miscarriages, affects 3-5% of couples trying to establish a family. Despite extensive evaluation, no factor is identified in ∼40% of cases. In this study, we investigated the possibility that submicroscopic chromosomal changes, not detectable by conventional cytogenetic analysis, exist in miscarriages with normal karyotypes (46,XY or 46,XX) from couples with idiopathic RPL.

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