Frequency of Prader–Willi syndrome in births conceived via assisted reproductive technology | Zendy

June-Anne Gold | Zendy; Chelsey Ruth | Zendy; Kathryn Osann | Zendy; Pamela Flodman | Zendy; Barbara McManus | Zendy; Hye Seung Lee | Zendy; Sandra Donkervoort | Zendy; Manaswitha Khare | Zendy; Elizabeth Roof | Zendy; Elizabeth Dykens | Zendy; Daniel J. Driscoll | Zendy; Merlin G. Butler | Zendy; Janalee Heinemann | Zendy; Suzanne B. Cassidy | Zendy; Virginia Kimonis | Zendy

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Frequency of Prader–Willi syndrome in births conceived via assisted reproductive technology

Author(s) -

June-Anne Gold,

Chelsey Ruth,

Kathryn Osann,

Pamela Flodman,

Barbara McManus,

Hye Seung Lee,

Sandra Donkervoort,

Manaswitha Khare,

Elizabeth Roof,

Elizabeth Dykens,

Daniel J. Driscoll,

Merlin G. Butler,

Janalee Heinemann,

Suzanne B. Cassidy,

Virginia Kimonis

Publication year - 2013

Publication title -

genetics in medicine

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 3.509

H-Index - 128

eISSN - 1530-0366

pISSN - 1098-3600

DOI - 10.1038/gim.2013.97

Subject(s) - assisted reproductive technology , medicine , obstetrics , gynecology , biology , pregnancy , infertility , genetics

Prader-Willi syndrome is an imprinting disorder characterized by typical facial, physical, and cognitive/behavioral features, resulting from lack of paternally expressed genes on chromosome 15q11.2-q13. Studies have suggested an increased risk of other imprinting disorders in children conceived by assisted reproductive techniques. This study was designed to determine the association between assisted reproductive technology and Prader-Willi syndrome.

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