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Prenatal Diagnosis of Fragile X Syndrome in a Twin Pregnancy Complicated by a Complete Retraction.
Prawer, Yael; Hunter, Matthew; Cronin, Sara; Ling, Ling; Aliaga Vera, Solange; Fahey, Michael; Gelfand, Nikki; Oertel, Ralph; Bartlett, Essra; Francis, David; Godler, David.
Afiliação
  • Prawer Y; Monash Genetics, Monash Health, Clayton, 3168 Victoria, Australia. yael.prawer@monashhealth.org.
  • Hunter M; Department of Paediatrics, Monash University, Clayton, 3168 Victoria, Australia. yael.prawer@monashhealth.org.
  • Cronin S; Monash Genetics, Monash Health, Clayton, 3168 Victoria, Australia. matthew.hunter@monashhealth.org.
  • Ling L; Department of Paediatrics, Monash University, Clayton, 3168 Victoria, Australia. matthew.hunter@monashhealth.org.
  • Aliaga Vera S; Cyto-Molecular Diagnostic Research Laboratory, Victorian Clinical Genetics Services and Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, 3052 Victoria, Australia. sara.cronin@vcgs.org.au.
  • Fahey M; Cyto-Molecular Diagnostic Research Laboratory, Victorian Clinical Genetics Services and Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, 3052 Victoria, Australia. ling.ling@mcri.edu.au.
  • Gelfand N; Cyto-Molecular Diagnostic Research Laboratory, Victorian Clinical Genetics Services and Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, 3052 Victoria, Australia. solange.aliagavera@mcri.edu.au.
  • Oertel R; Monash Genetics, Monash Health, Clayton, 3168 Victoria, Australia. michael.fahey@monashhealth.org.
  • Bartlett E; Monash Genetics, Monash Health, Clayton, 3168 Victoria, Australia. nikki.gelfand@monashhealth.org.
  • Francis D; Department of Paediatrics, Monash University, Clayton, 3168 Victoria, Australia. nikki.gelfand@monashhealth.org.
  • Godler D; Cyto-Molecular Diagnostic Research Laboratory, Victorian Clinical Genetics Services and Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, 3052 Victoria, Australia. ralph.oertel@vcgs.org.au.
Genes (Basel) ; 9(6)2018 Jun 07.
Article em En | MEDLINE | ID: mdl-29880767
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Genes (Basel) Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Austrália
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Genes (Basel) Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Austrália