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Exclusive paternal origin of new mutations in Apert syndrome.
Moloney, D M; Slaney, S F; Oldridge, M; Wall, S A; Sahlin, P; Stenman, G; Wilkie, A O.
Affiliation
  • Moloney DM; Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford, UK.
Nat Genet ; 13(1): 48-53, 1996 May.
Article in En | MEDLINE | ID: mdl-8673103
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Acrocephalosyndactylia / Receptors, Fibroblast Growth Factor / Receptor Protein-Tyrosine Kinases / Genomic Imprinting Type of study: Prognostic_studies Limits: Adult / Female / Humans / Male Language: En Journal: Nat Genet Journal subject: GENETICA MEDICA Year: 1996 Document type: Article Affiliation country: Reino Unido Country of publication: Estados Unidos
Search on Google
Add to My VHL
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Acrocephalosyndactylia / Receptors, Fibroblast Growth Factor / Receptor Protein-Tyrosine Kinases / Genomic Imprinting Type of study: Prognostic_studies Limits: Adult / Female / Humans / Male Language: En Journal: Nat Genet Journal subject: GENETICA MEDICA Year: 1996 Document type: Article Affiliation country: Reino Unido Country of publication: Estados Unidos