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Replication of 13q31.1 association in nonsyndromic cleft lip with cleft palate in Europeans.
Jia, Zhonglin; Leslie, Elizabeth J; Cooper, Margaret E; Butali, Azeez; Standley, Jennifer; Rigdon, Jennifer; Suzuki, Satoshi; Gongorjav, Ayana; Shonkhuuz, T Enkhtur; Natsume, Nagato; Shi, Bing; Marazita, Mary L; Murray, Jeffrey C.
Afiliação
  • Jia Z; State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
  • Leslie EJ; Department of Pediatrics, University of Iowa, Iowa City, Iowa.
  • Cooper ME; Department of Cleft Lip and Palate Surgery, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
  • Butali A; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Standley J; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Rigdon J; Department of Oral Pathology, Radiology, and Medicine, College of Dentistry, University of Iowa, Iowa City, Iowa.
  • Suzuki S; Department of Pediatrics, University of Iowa, Iowa City, Iowa.
  • Gongorjav A; Department of Pediatrics, University of Iowa, Iowa City, Iowa.
  • Shonkhuuz TE; Department of Pediatrics, University of Iowa, Iowa City, Iowa.
  • Natsume N; Division of Research and Treatment for Oral and Maxillofacial Congenital Anomalies, School of Dentistry, Aichi-Gakuin University, Japan.
  • Shi B; National Center for Maternal and Child Health, Ulaanbaatar, Mongolia.
  • Marazita ML; National Center for Maternal and Child Health, Ulaanbaatar, Mongolia.
  • Murray JC; Division of Research and Treatment for Oral and Maxillofacial Congenital Anomalies, School of Dentistry, Aichi-Gakuin University, Japan.
Am J Med Genet A ; 167A(5): 1054-1060, 2015 May.
Article em En | MEDLINE | ID: mdl-25786657
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 13 / Fenda Labial / Fissura Palatina / Predisposição Genética para Doença Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Female / Humans / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 13 / Fenda Labial / Fissura Palatina / Predisposição Genética para Doença Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Female / Humans / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article