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LAMM syndrome: two new patients with a novel mutation in FGF3 gene and additional clinical findings.
Basdemirci, Muserref; Zamani, Ayse G; Sener, Sevgi; Tassoker, Melek; Cetmili, Hayriye; Zamani, Adil; Aydogdu, Demet; Basdemirci, Ali; Yildirim, Mahmut S.
Afiliação
  • Basdemirci M; Department of Medical Genetics, Dr Ali Kemal Belviranli Maternity and Pediatric Hospital.
  • Zamani AG; Departments of Medical Genetics.
  • Sener S; Oral and Maxillofacial Radiology, Faculty of Dentistry, Necmettin Erbakan University, Konya, Turkey.
  • Tassoker M; Oral and Maxillofacial Radiology, Faculty of Dentistry, Necmettin Erbakan University, Konya, Turkey.
  • Cetmili H; Oral and Maxillofacial Radiology, Faculty of Dentistry, Necmettin Erbakan University, Konya, Turkey.
  • Zamani A; Chest Disease.
  • Aydogdu D; Radiology, Meram Medical Faculty.
  • Basdemirci A; Department of Anaesthesiology and Reanimation, Eregli State Hospital, Konya.
  • Yildirim MS; Departments of Medical Genetics.
Clin Dysmorphol ; 28(2): 81-85, 2019 Apr.
Article em En | MEDLINE | ID: mdl-30433887
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Dentárias / Fator 3 de Crescimento de Fibroblastos / Microtia Congênita / Perda Auditiva Neurossensorial / Orelha Interna Tipo de estudo: Diagnostic_studies Limite: Adult / Female / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Dentárias / Fator 3 de Crescimento de Fibroblastos / Microtia Congênita / Perda Auditiva Neurossensorial / Orelha Interna Tipo de estudo: Diagnostic_studies Limite: Adult / Female / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article