Preimplantation genetic diagnosis of X-linked diseases examined by indirect linkage analysis | Zendy

Irena Borgulová | Zendy; Martina Putzová | Zendy; I. A. Soldatova | Zendy; L. Krautova | Zendy; Ľubomíra Pecnová | Zendy; Josef Mika | Zendy; Radomír Křen | Zendy; P. Potuznikova | Zendy; D. Stejskal | Zendy

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Preimplantation genetic diagnosis of X-linked diseases examined by indirect linkage analysis

Author(s) -

Irena Borgulová,

Martina Putzová,

I. A. Soldatova,

L. Krautova,

Ľubomíra Pecnová,

Josef Mika,

Radomír Křen,

P. Potuznikova,

D. Stejskal

Publication year - 2015

Publication title -

bratislavské lekárske listy/bratislava medical journal

Language(s) - English

Resource type - Journals

eISSN - 1336-0345

pISSN - 0006-9248

DOI - 10.4149/bll_2015_103

Subject(s) - preimplantation genetic diagnosis , embryo transfer , genetics , embryo , proband , pregnancy , biology , gynecology , medicine , obstetrics , mutation , gene

Many centers of assisted reproduction in the Czech Republic offer preimplantation genetic diagnosis with fluorescent in situ hybridization (FISH) to couples requiring preimplantation genetic diagnosis (PGD) of X-linked diseases. However, this process results in discarding all male embryos and is not able to distinguish a carrier or healthy female embryo in X-linked recessive disorders.

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