Your browser doesn't support javascript.
loading
FOXP1-related intellectual disability syndrome: a recognisable entity.
Meerschaut, Ilse; Rochefort, Daniel; Revençu, Nicole; Pètre, Justine; Corsello, Christina; Rouleau, Guy A; Hamdan, Fadi F; Michaud, Jacques L; Morton, Jenny; Radley, Jessica; Ragge, Nicola; García-Miñaúr, Sixto; Lapunzina, Pablo; Bralo, Maria Palomares; Mori, Maria Ángeles; Moortgat, Stéphanie; Benoit, Valérie; Mary, Sandrine; Bockaert, Nele; Oostra, Ann; Vanakker, Olivier; Velinov, Milen; de Ravel, Thomy Jl; Mekahli, Djalila; Sebat, Jonathan; Vaux, Keith K; DiDonato, Nataliya; Hanson-Kahn, Andrea K; Hudgins, Louanne; Dallapiccola, Bruno; Novelli, Antonio; Tarani, Luigi; Andrieux, Joris; Parker, Michael J; Neas, Katherine; Ceulemans, Berten; Schoonjans, An-Sofie; Prchalova, Darina; Havlovicova, Marketa; Hancarova, Miroslava; Budisteanu, Magdalena; Dheedene, Annelies; Menten, Björn; Dion, Patrick A; Lederer, Damien; Callewaert, Bert.
Afiliación
  • Meerschaut I; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
  • Rochefort D; Department of Pediatrics, Ghent University Hospital, Ghent, Belgium.
  • Revençu N; Montreal Neurological Institute, McGill University, Montreal, Canada.
  • Pètre J; Centre de Génétique humaine, Cliniques Universitaires Saint-Luc, Université catholique de Louvain, Brussels, Belgium.
  • Corsello C; Centre de Génétique humaine, Cliniques Universitaires Saint-Luc, Université catholique de Louvain, Brussels, Belgium.
  • Rouleau GA; Montreal Neurological Institute, McGill University, Montreal, Canada.
  • Hamdan FF; Montreal Neurological Institute, McGill University, Montreal, Canada.
  • Michaud JL; CHU Sainte-Justine Research Center, Université de Montreal, Montreal, Canada.
  • Morton J; CHU Sainte-Justine Research Center, Université de Montreal, Montreal, Canada.
  • Radley J; West Midlands Regional Clinical Genetics Service and Birmingham Health Partners, Birmingham Women's Hospital NHS Foundation Trust, Birmingham Women's Hospital, Edgbaston, UK.
  • Ragge N; West Midlands Regional Clinical Genetics Service and Birmingham Health Partners, Birmingham Women's Hospital NHS Foundation Trust, Birmingham Women's Hospital, Edgbaston, UK.
  • García-Miñaúr S; West Midlands Regional Clinical Genetics Service and Birmingham Health Partners, Birmingham Women's Hospital NHS Foundation Trust, Birmingham Women's Hospital, Edgbaston, UK.
  • Lapunzina P; Instituto de Genética Médica y Molecular, Hospital Universitario La Paz, IdiPAZ, CIBERER, ISCIII, Madrid, Spain.
  • Bralo MP; Instituto de Genética Médica y Molecular, Hospital Universitario La Paz, IdiPAZ, CIBERER, ISCIII, Madrid, Spain.
  • Mori MÁ; Instituto de Genética Médica y Molecular, Hospital Universitario La Paz, IdiPAZ, CIBERER, ISCIII, Madrid, Spain.
  • Moortgat S; Instituto de Genética Médica y Molecular, Hospital Universitario La Paz, IdiPAZ, CIBERER, ISCIII, Madrid, Spain.
  • Benoit V; Centre de Génétique Humaine, Institut de Pathologie et de Génétique, Gosselies, Belgium.
  • Mary S; Centre de Génétique Humaine, Institut de Pathologie et de Génétique, Gosselies, Belgium.
  • Bockaert N; Centre de Génétique Humaine, Institut de Pathologie et de Génétique, Gosselies, Belgium.
  • Oostra A; Department of Pediatrics, Ghent University Hospital, Ghent, Belgium.
  • Vanakker O; Department of Pediatrics, Ghent University Hospital, Ghent, Belgium.
  • Velinov M; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
  • de Ravel TJ; Department of Pediatrics, Ghent University Hospital, Ghent, Belgium.
  • Mekahli D; NYS Institute for Basic Research in Developmental Disabilities, Staten Island, New York, USA.
  • Sebat J; Centre for Human Genetics, University Hospital Leuven, Leuven, Belgium.
  • Vaux KK; Department of Pediatric Nephrology, University Hospital Leuven, Leuven, Belgium.
  • DiDonato N; Beyster Center for Genomics of Psychiatric Diseases, University of California, San Diego, USA.
  • Hanson-Kahn AK; Departments of Medicine and Neurosciences, UC San Diego School of Medicine, San Diego, USA.
  • Hudgins L; Institut für Klinische Genetik, Technische Universität Dresden, Dresden, Deutschland.
  • Dallapiccola B; Department of Pediatrics, Division of Medical Genetics, Stanford University School of Medicine, California, USA.
  • Novelli A; Department of Pediatrics, Division of Medical Genetics, Stanford University School of Medicine, California, USA.
  • Tarani L; Laboratory of Medical Genetics, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Andrieux J; Laboratory of Medical Genetics, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Parker MJ; Department of Pediatrics and Child Neuropsychiatry, La Sapienza University, Rome, Italy.
  • Neas K; Institut de Génétique Médicale, Hospital Jeanne de Flandre, Lille, France.
  • Ceulemans B; Sheffield Clinical Genetics Service, Sheffield Children's Hospital, Sheffield, UK.
  • Schoonjans AS; Genetic Health Service NZ, Wellington, New Zealand.
  • Prchalova D; Department of Neurology-Pediatric Neurology, Antwerp University Hospital, Edegem, Belgium.
  • Havlovicova M; Department of Neurology-Pediatric Neurology, Antwerp University Hospital, Edegem, Belgium.
  • Hancarova M; Department of Biology and Medical Genetics, Charles University 2nd Faculty of Medicine and University Hospital Motol, Prague, Czech.
  • Budisteanu M; Department of Biology and Medical Genetics, Charles University 2nd Faculty of Medicine and University Hospital Motol, Prague, Czech.
  • Dheedene A; Department of Biology and Medical Genetics, Charles University 2nd Faculty of Medicine and University Hospital Motol, Prague, Czech.
  • Menten B; Psychiatry Research Laboratory, Prof Dr Alexandru Obregia Clinical Hospital of Psychiatry, Bercini, Romania.
  • Dion PA; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
  • Lederer D; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
  • Callewaert B; Montreal Neurological Institute, McGill University, Montreal, Canada.
J Med Genet ; 54(9): 613-623, 2017 09.
Article en En | MEDLINE | ID: mdl-28735298
Asunto(s)
Palabras clave
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Represoras / Factores de Transcripción Forkhead / Discapacidad Intelectual Tipo de estudio: Prognostic_studies Límite: Female / Humans / Male Idioma: En Revista: J Med Genet Año: 2017 Tipo del documento: Article País de afiliación: Bélgica Pais de publicación: Reino Unido
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Represoras / Factores de Transcripción Forkhead / Discapacidad Intelectual Tipo de estudio: Prognostic_studies Límite: Female / Humans / Male Idioma: En Revista: J Med Genet Año: 2017 Tipo del documento: Article País de afiliación: Bélgica Pais de publicación: Reino Unido