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TÍTULO: Genome sequencing and comprehensive rare-variant analysis of 465 families with neurodevelopmental disorders
AUTORES: Sanchis Juan, Alba; Megy, Karyn; Stephens, Jonathan; Ricaurte, Camila Armirola; Dewhurst, Eleanor; Low, Kayyi; French, Courtney E.; Grozeva, Detelina; Stirrups, Kathleen; Erwood, Marie; McTague, Amy; Penkett, Christopher J.; Shamardina, Olga; Tuna, Salih; Daugherty, Louise C.; Gleadall, Nicholas; Duarte, Sofia T.; Hedrera Fernandez, Antonio; Vogt, Julie; Ambegaonkar, Gautam; Chitre, Manali; Josifova, Dragana; Kurian, Manju A.; Parker, Alasdair; Rankin, Julia; Reid, Evan; Wakeling, Emma; Wassmer, Evangeline; NIHR BioResource, F. Lucy; Raymond, F. Lucy; Carss, Keren J.; ...Mais
PUBLICAÇÃO: 2023, FONTE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 110, NÚMERO: 8
INDEXADO EM: Scopus WOS