Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Learning and NSD1[original query] |
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Psychosocial, cognitive, and motor functioning in patients with suspected Sotos syndrome: a comparison between patients with and without NSD1 gene alterations. Developmental medicine and child neurology 2006 Jul 48 (7): 582-8. de Boer L, Röder I, Wit J |
Heterogeneity of NSD1 alterations in 116 patients with Sotos syndrome. Human mutation 2007 Nov 28 (11): 1098-107. Saugier-Veber Pascale, Bonnet Céline, Afenjar Alexandra, Drouin-Garraud Valérie, Coubes Christine, Fehrenbach Séverine, Holder-Espinasse Muriel, Roume Joëlle, Malan Valérie, Portnoi Marie-France, Jeanne Nicolas, Baumann Clarisse, Héron Delphine, David Albert, Gérard Marion, Bonneau Dominique, Lacombe Didier, Cormier-Daire Valérie, Billette de Villemeur Thierry, Frébourg Thierry, Bürglen Lyd |
Mutation analysis of the NSD1 gene in patients with autism spectrum disorders and macrocephaly. BMC medical genetics 2007 8 (1): 68. Buxbaum Joseph D, Cai Guiqing, Nygren Gudrun, Chaste Pauline, Delorme Richard, Goldsmith Juliet, Råstam Maria, Silverman Jeremy M, Hollander Eric, Gillberg Christopher, Leboyer Marion, Betancur Catali |
The Association of Scoliosis and NSD1 Gene Deletion in Sotos Syndrome Patients. Spine 2020 12 46 (13): E726-E733. Machida Masafumi, Katoh Hiroyuki, Machida Masayoshi, Miyake Atsushi, Taira Katsuaki, Ohashi Hirofu |
Cognitive, adaptive and behavioral profile in Sotos syndrome children with 5q35 microdeletion or intragenic variants. American journal of medical genetics. Part A 2023 4 . Siracusano Martina, Riccioni Assia, Frattale Ilaria, Arturi Lucrezia, Dante Caterina, Galasso Cinzia, Gialloreti Leonardo Emberti, Conteduca Giuseppina, Testa Barbara, Malacarne Michela, Coviello Domenico, Mazzone Lui |
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