Percorrer por autor Saraiva, JM

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DataTítuloAutor(es)TipoAcesso
2012Avaliação e Investigação Etiológica do Atraso do Desenvolvimento Psicomotor / Défice IntelectualOliveira, R; Rodrigues, F; Venâncio, M; Saraiva, JM; Fernandes, BarticleopenAccess
2013Description of an autosomal dominant form of Kabuki syndrome by mutation in MLL2 geneSantos, MI; Beleza-Meireles, A; Loureiro, S; Fonseca, M; Reis, CF; Rodrigues, F; Ramos, F; Ramos, L; Cardoso, E; Saraiva, JMarticleopenAccess
2013Gain-of-function mutations in the phosphatidylserine synthase 1 (PTDSS1) gene cause Lenz-Majewski syndromeSousa, SB; Jenkins, D; Chanudet, E; Tasseva, G; Ishida, M; Anderson, G; Docker, J; Ryten, M; Sá, J; Saraiva, JM; Barnicoat, A; Scott, R; Calder, A; Wattanasirichaigoon, D; Chrzanowska, K; Simandlová, M; Van Maldergem, L; Stanier, P; Beales, PL; Vance, JE; Moore, GEarticleopenAccess
Jan-2014Intellectual disability, coarse face, relative macrocephaly, and cerebellar hypotrophy in two sistersSousa, SB; Ramos, F; Garcia, P; Pais, RP; Paiva, C; Beales, PL; Moore, GE; Saraiva, JM; Hennekam, RCarticleopenAccess
2013Intellectual disability, unusual facial morphology and hand anomalies in sibsSousa, SB; Venâncio, M; Chanudet, E; Palmer, R; Ramos, L; Beales, PL; Moore, GE; Saraiva, JM; Hennekam, RCarticleopenAccess
2013Juvenile polyposis of infancy in a child with deletion of BMPR1A and PTEN genes: Surgical approachOliveira, PH; Cunha, C; Almeida, S; Ferreira, R; Maia, S; Saraiva, JM; Lopes, MFarticleopenAccess
2012MÓDULO 6 - Genética, Metabólicas, Neuroimagem/EEG e PedopsiquiatriaBento, C; Rodrigues, F; Oliveira, G; Lopes, MF; Brito, MJ; Saraiva, JM; Veiga, R; Pais, R; Pena, B; Veiga, L; Loureiro, MJ; Garrido, J; Ramos, F; Sá, J; Garcia, PbookopenAccess
6-Nov-2014Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndromeThomas, AC; Williams, H; Setó-Salvia, N; Bacchelli, C; Jenkins, D; O'Sullivan, M; Mengrelis, K; Ishida, M; Ocaka, L; Chanudet, E; James, C; Lescai, F; Anderson, G; Morrogh, D; Ryten, M; Duncan, AJ; Pai, YJ; Saraiva, JM; Ramos, F; Farren, B; Saunders, D; Vernay, B; Gissen, P; Straatmaan-Iwanowska, A; Baas, F; Wood, NW; Hersheson, J; Houlden, H; Hurst, J; Scott, R; Bitner-Glindzicz, M; Moore, GE; Sousa, SB; Stanier, ParticleopenAccess
2013Non-syndromic Sensorineural Prelingual Deafness: The Importance of Genetic Counseling in Demystifying Parents’ Beliefs About the Cause of Their Children’s DeafnessRodrigues, F; Paneque, M; Reis, C; Venâncio, M; Sequeiros, J; Saraiva, JMarticleopenAccess
Out-2014Oculo-auriculo-vertebral spectrum: a review of the literature and genetic updateBeleza-Meireles, AF; Clayton-Smith, J; Saraiva, JM; Tassabehji, MarticleopenAccess
2012Reduced elastogenesis: a clue to the arteriosclerosis and emphysematous changes in Schimke immuno-osseous dysplasia?Morimoto, M; Yu, Z; Stenzel, P; Clewing, JM; Najafian, B; Mayfield, C; Hendson, G; Weinkauf, JG; Gormley, AK; Saraiva, JMarticleopenAccess
2014Regarding the article "Adults with Down syndrome: characterization of a Portuguese sample"Saraiva, JMarticleopenAccess
2014Regarding the article "Adults with Down syndrome: characterization of a Portuguese sample"Saraiva, JMarticleopenAccess
1999Schimke immuno-osseous dysplasia: case report and review of 25 patientsSaraiva, JM; Dinis, A; Resende, C; Faria, E; Gomes, C; Correia, AJ; Gil, J; Fonseca, NarticleopenAccess