Comparing a Novel Malformation Syndrome Caused by Pathogenic Variants in <i>FBRSL1</i> to AUTS2 Syndrome.

Pauli, Silke; Berger, Hanna; Ufartes, Roser; Borchers, Annette

Comparing a Novel Malformation Syndrome Caused by Pathogenic Variants in FBRSL1 to AUTS2 Syndrome.

Pauli, Silke; Berger, Hanna; Ufartes, Roser; Borchers, Annette.

Afiliación

Pauli S; Institute of Human Genetics, University Medical Center Göttingen, Göttingen, Germany.
Berger H; Faculty of Biology, Molecular Embryology, Philipps-University Marburg, Marburg, Germany.
Ufartes R; Institute of Human Genetics, University Medical Center Göttingen, Göttingen, Germany.
Borchers A; Faculty of Biology, Molecular Embryology, Philipps-University Marburg, Marburg, Germany.

Front Cell Dev Biol ; 9: 779009, 2021.

Article en En | MEDLINE | ID: mdl-34805182

Palabras clave

AUTS2; FBRSL1; embryonic development; malformation syndrome; polycomb complex

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Cell Dev Biol Año: 2021 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Suiza

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