Recurrent X chromosome-linked deletions: discovery of new genetic factors in male infertility.

Lo Giacco, D; Chianese, C; Ars, E; Ruiz-Castañé, E; Forti, G; Krausz, C

Lo Giacco, D; Chianese, C; Ars, E; Ruiz-Castañé, E; Forti, G; Krausz, C.

Affiliation

Lo Giacco D; Molecular Biology Laboratory, Fundació Puigvert Universitat Autònoma de Barcelona, Instituto de Investigaciones Biomédicas Sant Pau (IIB-Sant Pau), Barcelona, Spain.

J Med Genet ; 51(5): 340-4, 2014 May.

Article in En | MEDLINE | ID: mdl-24421283

Subject(s)

Chromosomes, Human, X; Infertility, Male/genetics; Sequence Deletion; Azoospermia/genetics; Case-Control Studies; Gene Dosage; Genes, X-Linked; Genetic Association Studies; Humans; Male; Pedigree; Spermatogenesis/genetics

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sequence Deletion / Chromosomes, Human, X / Infertility, Male Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans / Male Language: En Journal: J Med Genet Year: 2014 Type: Article Affiliation country: Spain

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