Concerns regarding the potentially causal role of FANCA heterozygous variants in human primary ovarian insufficiency. | Hum Genet;140(4): 691-694, 2021 04. | MEDLINE

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Concerns regarding the potentially causal role of FANCA heterozygous variants in human primary ovarian insufficiency.

Heddar, Abdelkader; Misrahi, Micheline.

Affiliation

Heddar A; Faculté de Médecine; Unité de Génétique Moléculaire Des Maladies Métaboliques Et de La Reproduction, APHP Hôpitaux Universitaires Paris-Saclay, Université Paris Saclay, Hôpital Bicêtre, 94275, Le Kremlin-Bicêtre, France.
Misrahi M; Université Paris Saclay, UMR-S 1193, INSERM, Hôpital Paul Brousse, Villejuif, France.

Hum Genet ; 140(4): 691-694, 2021 04.

Article in En | MEDLINE | ID: mdl-33151384

Subject(s)

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Primary Ovarian Insufficiency Limits: Female / Humans Language: En Journal: Hum Genet Year: 2021 Document type: Article Affiliation country:

Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Primary Ovarian Insufficiency Limits: Female / Humans Language: En Journal: Hum Genet Year: 2021 Document type: Article Affiliation country: