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Genomic imbalances in craniofacial microsomia.
Spineli-Silva, Samira; Sgardioli, Ilária C; Dos Santos, Ana P; Bergamini, Luna L; Monlleó, Isabella L; Fontes, Marshall I B; Félix, Têmis M; Ribeiro, Erlane M; Xavier, Ana C; Lustosa-Mendes, Elaine; Gil-da-Silva-Lopes, Vera L; Vieira, Tarsis P.
Affiliation
  • Spineli-Silva S; Department of Medical Genetics and Genomic Medicine, School of Medical Sciences, State University of Campinas (Unicamp), Campinas, Brazil.
  • Sgardioli IC; Department of Medical Genetics and Genomic Medicine, School of Medical Sciences, State University of Campinas (Unicamp), Campinas, Brazil.
  • Dos Santos AP; Department of Medical Genetics and Genomic Medicine, School of Medical Sciences, State University of Campinas (Unicamp), Campinas, Brazil.
  • Bergamini LL; Faculty of Medicine, Federal University of Alagoas (UFAL), Maceió, Brazil.
  • Monlleó IL; Faculty of Medicine, Federal University of Alagoas (UFAL), Maceió, Brazil.
  • Fontes MIB; Clinical Genetics Service, University Hospital, Federal University of Alagoas (UFAL), Maceió, Brazil.
  • Félix TM; Clinical Genetics Service, University Hospital, Federal University of Alagoas (UFAL), Maceió, Brazil.
  • Ribeiro EM; Medical Genetics Service, Clinical Hospital of Porto Alegre (HCPA), Porto Alegre, Brazil.
  • Xavier AC; Medical Genetics Service, Hospital Infantil Albert Sabin (HIAS), Fortaleza, Brazil.
  • Lustosa-Mendes E; Centre for Research and Rehabilitation of Lip and Palate Lesions, Centrinho Prefeito Luiz Gomes, Joinville, Brazil.
  • Gil-da-Silva-Lopes VL; Assistance Centre for Cleft Lip and Palate - CAIF-AFISSUR, Curitiba, Brazil.
  • Vieira TP; Department of Medical Genetics and Genomic Medicine, School of Medical Sciences, State University of Campinas (Unicamp), Campinas, Brazil.
Am J Med Genet C Semin Med Genet ; 184(4): 970-985, 2020 12.
Article in En | MEDLINE | ID: mdl-33215817
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Goldenhar Syndrome / Heart Defects, Congenital Limits: Humans Language: En Journal: Am J Med Genet C Semin Med Genet Journal subject: GENETICA MEDICA Year: 2020 Document type: Article Affiliation country: Brasil Country of publication: Estados Unidos
Fulltext
Add to My VHL
Print
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Goldenhar Syndrome / Heart Defects, Congenital Limits: Humans Language: En Journal: Am J Med Genet C Semin Med Genet Journal subject: GENETICA MEDICA Year: 2020 Document type: Article Affiliation country: Brasil Country of publication: Estados Unidos