ReP USP - Resultado da busca

Filtros : "FENÓTIPOS" "Faculty of Medicine, Human Genetics Unit, University of Colombo, Sri Lanka" "HRAC" Removidos: "NUTRIÇÃO" "HRAC-DVSAUD-61" Limpar

Filtros

Autores USP
- costa, antonio richieri da (~1)
Ano de publicação
- 2017 (~1)
Assuntos
- análise facial (~1)
- fenótipos (~1)
Idioma
- inglês (~1)
Título da fonte
- american journal of medical genetics. part a (~1)
Editora
Nome do evento
País de publicação
- estados unidos (~1)
Grupo de pesquisa
Agência de fomento
Indexado em
- indexado no embase (elsevier) (~1)
- indexado no medline/pubmed (nlm) (~1)
- indexado no pubmed (~1)
- indexado no web of science (clarivate analytics) (~1)
Colaboração institucional
Afiliação dos autores externos normalizada
Afiliação dos autores externos não normalizada
- center for research on genomics and global health, national human genome research institute, the national institutes of health, bethesda, maryland, usa (1)
- center of excellence for medical genetics, faculty of medicine, department of pediatrics, chulalongkorn university, bangkok, thailand (1)
- center of human genetics/school of medicine and pharmacy, college of medicine and health sciences, university of rwanda, kigali, rwanda (1)
- department of medical genetics, university of campinas, são paulo, brazil (1)
- department of paediatrics college of medicine, university of lagos, lagos university teaching, lagos, nigeria (1)

Artigo de periodico
22q11.2 deletion syndrome in diverse populations (2017)
Kruszka, Paul; Addissie, Yonit A.; McGinn, Daniel E.; Porras, Antonio R.; Biggs, Elijah; Share, Matthew; Crowley, T. Blaine; Chung, Brian H. Y.; Mok, Gary T. K.; Mak, Christopher C. Y.; Muthukumarasamy, Premala; Thong, Meow-Keong; Sirisena, Nirmala D.; Dissanayake, Vajira H. W.; Paththinige, C. Sampath; Prabodha, L. B. Lahiru; Mishra, Rupesh; Shotelersuk, Vorasuk; Ekure, Ekanem Nsikak; Sokunbi, Ogochukwu Jidechukwu; Kalu, Nnenna; Ferreira, Carlos R.; Duncan, Jordann-Mishael; Patil, Siddaramappa Jagdish; Jones, Kelly L.; Kaplan, Julie D.; Abdul-Rahman, Omar A.; Uwineza, Annette; Mutesa, Leon; Moresco, Angélica; Obregon, María Gabriela; Richieri-Costa, Antonio; Gil-da-Silva-Lopes, Vera Lúcia; Adeyemo, Adebowale A.; Summar, Marshall; Zackai, Elaine H.; McDonald-McGinn, Donna M.; Linguraru, Marius George; Muenke, Maximilian
Fonte: American Journal of Medical Genetics. Part A. Unidade: HRAC
Assuntos: ANÁLISE FACIAL, FENÓTIPOS, ANÁLISE FACIAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KRUSZKA, Paul et al. 22q11.2 deletion syndrome in diverse populations. American Journal of Medical Genetics. Part A, v. 173, n. 4, p. 879-888, 2017Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.38199. Acesso em: 23 jun. 2024.
APA
Kruszka, P., Addissie, Y. A., McGinn, D. E., Porras, A. R., Biggs, E., Share, M., et al. (2017). 22q11.2 deletion syndrome in diverse populations. American Journal of Medical Genetics. Part A, 173( 4), 879-888. doi:10.1002/ajmg.a.38199
NLM
Kruszka P, Addissie YA, McGinn DE, Porras AR, Biggs E, Share M, Crowley TB, Chung BHY, Mok GTK, Mak CCY, Muthukumarasamy P, Thong M-K, Sirisena ND, Dissanayake VHW, Paththinige CS, Prabodha LBL, Mishra R, Shotelersuk V, Ekure EN, Sokunbi OJ, Kalu N, Ferreira CR, Duncan J-M, Patil SJ, Jones KL, Kaplan JD, Abdul-Rahman OA, Uwineza A, Mutesa L, Moresco A, Obregon MG, Richieri-Costa A, Gil-da-Silva-Lopes VL, Adeyemo AA, Summar M, Zackai EH, McDonald-McGinn DM, Linguraru MG, Muenke M. 22q11.2 deletion syndrome in diverse populations [Internet]. American Journal of Medical Genetics. Part A. 2017 ; 173( 4): 879-888.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1002/ajmg.a.38199
Vancouver
Kruszka P, Addissie YA, McGinn DE, Porras AR, Biggs E, Share M, Crowley TB, Chung BHY, Mok GTK, Mak CCY, Muthukumarasamy P, Thong M-K, Sirisena ND, Dissanayake VHW, Paththinige CS, Prabodha LBL, Mishra R, Shotelersuk V, Ekure EN, Sokunbi OJ, Kalu N, Ferreira CR, Duncan J-M, Patil SJ, Jones KL, Kaplan JD, Abdul-Rahman OA, Uwineza A, Mutesa L, Moresco A, Obregon MG, Richieri-Costa A, Gil-da-Silva-Lopes VL, Adeyemo AA, Summar M, Zackai EH, McDonald-McGinn DM, Linguraru MG, Muenke M. 22q11.2 deletion syndrome in diverse populations [Internet]. American Journal of Medical Genetics. Part A. 2017 ; 173( 4): 879-888.[citado 2024 jun. 23 ] Available from: https://doi.org/10.1002/ajmg.a.38199

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