Mette Gilling
AuthID: R-00F-GZK
1
TÃTULO: Linked Registries: Connecting Rare Diseases Patient Registries through a Semantic Web Layer Full Text
AUTORES: Pedro Sernadela; Lorena Gonzalez Castro; Claudio Carta; Eelke van der Horst; Pedro Lopes; Rajaram Kaliyaperumal; Mark Thompson; Rachel Thompson; Nuria Queralt Rosinach; Estrella Lopez; Libby Wood; Agata Robertson; Claudia Lamanna; Mette Gilling; Michael Orth; Roxana Merino Martinez; Manuel Posada; Domenica Taruscio; Hanns Lochmuller; Peter Robinson; ...Mais
PUBLICAÇÃO: 2017, FONTE: BIOMED RESEARCH INTERNATIONAL, VOLUME: 2017
AUTORES: Pedro Sernadela; Lorena Gonzalez Castro; Claudio Carta; Eelke van der Horst; Pedro Lopes; Rajaram Kaliyaperumal; Mark Thompson; Rachel Thompson; Nuria Queralt Rosinach; Estrella Lopez; Libby Wood; Agata Robertson; Claudia Lamanna; Mette Gilling; Michael Orth; Roxana Merino Martinez; Manuel Posada; Domenica Taruscio; Hanns Lochmuller; Peter Robinson; ...Mais
PUBLICAÇÃO: 2017, FONTE: BIOMED RESEARCH INTERNATIONAL, VOLUME: 2017
2
TÃTULO: Dysfunction of the Heteromeric KV7.3/KV7.5 Potassium Channel is Associated with Autism Spectrum Disorders Full Text
AUTORES: Mette Gilling; Hanne B Rasmussen; Kirstine Calloe; Ana F Sequeira; Marta Baretto; Guiomar Oliveira; Joana Almeida; Marlene B Lauritsen; Reinhard Ullmann; Susanne E Boonen; Karen Brondum-Nielsen; Vera M Kalscheuer; Zeynep Tümer; Astrid M Vicente; Nicole Schmitt; Niels Tommerup;
PUBLICAÇÃO: 2013, FONTE: Front. Genet. - Frontiers in Genetics, VOLUME: 4
AUTORES: Mette Gilling; Hanne B Rasmussen; Kirstine Calloe; Ana F Sequeira; Marta Baretto; Guiomar Oliveira; Joana Almeida; Marlene B Lauritsen; Reinhard Ullmann; Susanne E Boonen; Karen Brondum-Nielsen; Vera M Kalscheuer; Zeynep Tümer; Astrid M Vicente; Nicole Schmitt; Niels Tommerup;
PUBLICAÇÃO: 2013, FONTE: Front. Genet. - Frontiers in Genetics, VOLUME: 4
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TÃTULO: A 3.2Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia Full Text
AUTORES: Mette Gilling; Marlene Briciet Lauritsen; Morten Moller; Karen Friis Henriksen; Astrid Vicente ; Guiomar Oliveira ; Christina Cintin; Hans Eiberg; Paal Skyt Andersen; Ole Mors; Thomas Rosenberg; Karen Brondum Nielsen; Rodney M J Cotterill; Claes Lundsteen; Hans Hilger Ropers; Reinhard Ullmann; Iben Bache; Zeynep Tuemer; Niels Tommerup;
PUBLICAÇÃO: 2008, FONTE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 16, NÚMERO: 3
AUTORES: Mette Gilling; Marlene Briciet Lauritsen; Morten Moller; Karen Friis Henriksen; Astrid Vicente ; Guiomar Oliveira ; Christina Cintin; Hans Eiberg; Paal Skyt Andersen; Ole Mors; Thomas Rosenberg; Karen Brondum Nielsen; Rodney M J Cotterill; Claes Lundsteen; Hans Hilger Ropers; Reinhard Ullmann; Iben Bache; Zeynep Tuemer; Niels Tommerup;
PUBLICAÇÃO: 2008, FONTE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 16, NÚMERO: 3
