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Association between polymorphisms at the GREM1 locus and the risk of nonsyndromic cleft lip with or without cleft palate in the Polish population.
Mostowska, Adrianna; Hozyasz, Kamil K; Wójcicki, Piotr; Zukowski, Kacper; Dabrowska, Anna; Lasota, Agnieszka; Zadurska, Malgorzata; Radomska, Agnieszka; Dunin-Wilczynska, Izabela; Jagodzinski, Pawel P.
Afiliação
  • Mostowska A; Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poznan, Poland.
  • Hozyasz KK; Department of Paediatrics, Institute of Mother and Child, Warsaw, Poland.
  • Wójcicki P; University Clinic of Medical Academy in Wroclaw and Department of Plastic Surgery Specialist Medical Center in Polanica Zdroj, Poland.
  • Zukowski K; Department of Animal Genetics and Breeding, National Research Institute of Animal Production, Balice, Poland.
  • Dabrowska A; Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poznan, Poland.
  • Lasota A; Department of Jaw Orthopaedics, Medical University of Lublin, Lublin, Poland.
  • Zadurska M; Department of Orthodontics, Institute of Dentistry, The Medical University of Warsaw, Poland.
  • Radomska A; Department of Orthodontics, Institute of Dentistry, The Medical University of Warsaw, Poland.
  • Dunin-Wilczynska I; Department of Jaw Orthopaedics, Medical University of Lublin, Lublin, Poland.
  • Jagodzinski PP; Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poznan, Poland.
Birth Defects Res A Clin Mol Teratol ; 103(10): 847-56, 2015 Oct.
Article em En | MEDLINE | ID: mdl-26043427
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo Genético / Cromossomos Humanos Par 15 / Fenda Labial / Fissura Palatina / Peptídeos e Proteínas de Sinalização Intercelular / Loci Gênicos Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn País/Região como assunto: Europa Idioma: En Revista: Birth Defects Res A Clin Mol Teratol Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Polônia
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo Genético / Cromossomos Humanos Par 15 / Fenda Labial / Fissura Palatina / Peptídeos e Proteínas de Sinalização Intercelular / Loci Gênicos Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn País/Região como assunto: Europa Idioma: En Revista: Birth Defects Res A Clin Mol Teratol Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Polônia