ESHRE PGT Consortium data collection XXI: PGT analyses in 2018.

Spinella, F; Bronet, F; Carvalho, F; Coonen, E; De Rycke, M; Rubio, C; Goossens, V; Van Montfoort, A

Spinella, F; Bronet, F; Carvalho, F; Coonen, E; De Rycke, M; Rubio, C; Goossens, V; Van Montfoort, A.

Afiliação

Spinella F; Eurofins GENOMA Group srl, Molecular Genetics Laboratories, Rome, Italy.
Bronet F; IVIRMA-IVI Madrid, Madrid, Spain.
Carvalho F; Genetics-Department of Pathology, Faculty of Medicine, University of Porto, Porto, Portugal.
Coonen E; i3s-Instituto de Investigação e Inovação em Saúde, University of Porto, Porto, Portugal.
De Rycke M; Department of Clinical Genetics, GROW School for Oncology and Developmental Biology, Maastricht University Medical Centre, Maastricht, The Netherlands.
Rubio C; Centre for Medical Genetics, UZ Brussel, Brussels, Belgium.
Goossens V; PGT-A Research, Igenomix, Valencia, Spain.
Van Montfoort A; ESHRE Central Office, Strombeek-Bever, Belgium.

Hum Reprod Open ; 2023(2): hoad010, 2023.

Article em En | MEDLINE | ID: mdl-37091225

Palavras-chave

PGT; aneuploidy; comprehensive genetic testing; data collection; human embryo; monogenic disorders; registry; structural rearrangements

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article