المؤلفون: Mota S, Sá C, Gonçalves Rocha M, Pereira A

المصدر: Ecos do Minho, Vol 16 (2021)

مصطلحات موضوعية: Medicine, Pediatrics, RJ1-570

وصف الملف: electronic resource

العلاقة: https://apminho.com/images/pdf/2021/08.Nem%20toda%20a%20plagiocefalia%20%C3%A9%20posicional.pdfTest; https://doaj.org/toc/1646-4745Test

الوصول الحر: https://doaj.org/article/7b212097324a41b1b749a06b4a268ce1Test

المؤلفون: Sousa, A, Moldovan, O, Lebreiro, A, Bourbon, M, António, N, Rato, Q, Rodrigues, P, Toste, A, Gonçalves Rocha, M, Oliveira, R, Granja, S, Cruz, C, Almeida, J, Martins, E

المساهمون: Instituto de Investigação e Inovação em Saúde

مصطلحات موضوعية: Genetic testing, Inherited cardiovascular diseases, Cardiology, Genetic Counseling, Humans, Syndrome

وصف الملف: application/pdf

العلاقة: Revista Portuguesa de Cardiologia, vol.39(10), p. 597-610; https://www.sciencedirect.com/science/article/pii/S0870255120303541?via%3DihubTest; https://hdl.handle.net/10216/143571Test

الإتاحة: https://doi.org/10.1016/j.repc.2020.03.016Test
https://hdl.handle.net/10216/143571Test

المؤلفون: Lopes, F, Soares, G, Gonçalves-Rocha, M, Pinto-Basto, JM, Maciel, P

مصطلحات موضوعية: Haploinsuficiência, Perturbações do Neurodesenvolvimento/genética

العلاقة: Front Genet. 2017 Oct 9;8:143.; http://hdl.handle.net/10400.23/1217Test

الإتاحة: https://doi.org/10.3389/fgene.2017.00143Test
http://hdl.handle.net/10400.23/1217Test

المؤلفون: Ribeiro, B, Igreja, J, Gonçalves-Rocha, M, Cadilhe, A

مصطلحات موضوعية: Síndrome de Goldenhar

العلاقة: BMJ Case Rep. 2016 Jun 21;2016. pii: bcr2016215258.; http://hdl.handle.net/10400.23/1057Test

الإتاحة: https://doi.org/10.1136/bcr-2016-215258Test
http://hdl.handle.net/10400.23/1057Test

المؤلفون: Araújo, C, Gonçalves-Rocha, M, Resende, C, Vieira, AP, Brito, C

مصطلحات موضوعية: Alopécia, Ictiose, Fotofobia, Síndrome, Anomalias Congénitas Múltiplas, Dermatite Atópica

العلاقة: Case Rep Med. 2015;2015:450937.; http://hdl.handle.net/10400.23/834Test

الإتاحة: http://hdl.handle.net/10400.23/834Test

المؤلفون: Rymen, D, Peanne, R, Millón, MB, Race, V, Sturiale, L, Garozzo, D, Mills, P, Clayton, P, Asteggiano, CG, Quelhas, D, Cansu, A, Martins, E, Nassogne, MC, Gonçalves-Rocha, M, Topaloglu, H, Jaeken, J, Foulquier, F, Matthijs, G

المصدر: PLoS Genetics , 9 (12) , Article e1003989. (2013)

وصف الملف: application/pdf

العلاقة: https://discovery.ucl.ac.uk/id/eprint/1421754/1/journal.pgen.1003989.pdfTest; https://discovery.ucl.ac.uk/id/eprint/1421754Test/

الإتاحة: https://discovery.ucl.ac.uk/id/eprint/1421754/1/journal.pgen.1003989.pdfTest
https://discovery.ucl.ac.uk/id/eprint/1421754Test/

المؤلفون: Gonçalves-Rocha, M., Silva, J., Fortuna, A., Soares, G.

العلاقة: Nascer e Crescer 2008; 17(4): 268-269; http://hdl.handle.net/10400.16/1171Test

الإتاحة: http://hdl.handle.net/10400.16/1171Test

المؤلفون: Gonçalves-Rocha, M., Silva, J., Fortuna, A., Soares, G.

المصدر: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=od______3056::abf1a51a727d1edaafaf58060e299d93Test

المؤلفون: Gonçalves-Rocha, M., Silva, J., Fortuna, A., Soares, G.

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=od______2346::abf1a51a727d1edaafaf58060e299d93Test
https://hdl.handle.net/10400.16/1171Test

المؤلفون: Lopes, F., Soares, G., Gonçalves-Rocha, M., Pinto-Basto, J., Maciel, P.

المساهمون: Repositório Científico do Centro Hospitalar Universitário de Santo António

مصطلحات موضوعية: EBF3, intellectual disability, syndrome, 10qter deletion, hypotonia, movement disorder

وصف الملف: application/pdf

العلاقة: Front Genet. 2017 Oct 9;8:143; 1664-8021

الإتاحة: http://hdl.handle.net/10400.16/2222Test