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ZSWIM7 Is Associated With Human Female Meiosis and Familial Primary Ovarian Insufficiency.
McGlacken-Byrne, Sinéad M; Le Quesne Stabej, Polona; Del Valle, Ignacio; Ocaka, Louise; Gagunashvili, Andrey; Crespo, Berta; Moreno, Nadjeda; James, Chela; Bacchelli, Chiara; Dattani, Mehul T; Williams, Hywel J; Kelberman, Dan; Achermann, John C; Conway, Gerard S.
Affiliation
  • McGlacken-Byrne SM; Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, University College London, London WC1N 1EH, UK.
  • Le Quesne Stabej P; Institute for Women's Health, University College London, London WC1N 1EH, UK.
  • Del Valle I; GOSgene, Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, University College London, London WC1N 1EH, UK.
  • Ocaka L; Department of Molecular Medicine and Pathology, University of Auckland, Auckland, New Zealand.
  • Gagunashvili A; Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, University College London, London WC1N 1EH, UK.
  • Crespo B; GOSgene, Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, University College London, London WC1N 1EH, UK.
  • Moreno N; GOSgene, Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, University College London, London WC1N 1EH, UK.
  • James C; Developmental Biology and Cancer, UCL Great Ormond Street Institute of Child Health, University College London, London WC1N 1EH, UK.
  • Bacchelli C; Developmental Biology and Cancer, UCL Great Ormond Street Institute of Child Health, University College London, London WC1N 1EH, UK.
  • Dattani MT; GOSgene, Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, University College London, London WC1N 1EH, UK.
  • Williams HJ; GOSgene, Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, University College London, London WC1N 1EH, UK.
  • Kelberman D; Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, University College London, London WC1N 1EH, UK.
  • Achermann JC; Division of Cancer and Genetics, Genetic and Genomic Medicine, Cardiff University, Cardiff CF14 4AY, UK.
  • Conway GS; GOSgene, Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, University College London, London WC1N 1EH, UK.
J Clin Endocrinol Metab ; 107(1): e254-e263, 2022 01 01.
Article de En | MEDLINE | ID: mdl-34402903
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Ovogenèse / Insuffisance ovarienne primitive / Protéines de liaison à l'ADN / Aménorrhée / Méiose Type d'étude: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limites: Adolescent / Child / Female / Humans Langue: En Journal: J Clin Endocrinol Metab Année: 2022 Type de document: Article Pays d'affiliation: Royaume-Uni Pays de publication: États-Unis d'Amérique
Texte intégral
Ajouter à My VHL
Imprimer
XML
PubMed Links
Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Ovogenèse / Insuffisance ovarienne primitive / Protéines de liaison à l'ADN / Aménorrhée / Méiose Type d'étude: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limites: Adolescent / Child / Female / Humans Langue: En Journal: J Clin Endocrinol Metab Année: 2022 Type de document: Article Pays d'affiliation: Royaume-Uni Pays de publication: États-Unis d'Amérique