22q11.2 deletion syndrome in diverse populations (2017)
- Authors:
- 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
- Autor USP: COSTA, ANTONIO RICHIERI DA - HRAC
- Unidade: HRAC
- DOI: 10.1002/ajmg.a.38199
- Subjects: ANÁLISE FACIAL; FENÓTIPOS; ANÁLISE FACIAL
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: American Journal of Medical Genetics. Part A
- Volume/Número/Paginação/Ano: v. 173, n. 4, p. 879-888, Feb. 2017
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: green
-
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: 27 abr. 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 abr. 27 ] 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 abr. 27 ] Available from: https://doi.org/10.1002/ajmg.a.38199 - Tibial hemimelia-split hand/foot syndrome, report of a brazilian family
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Informações sobre o DOI: 10.1002/ajmg.a.38199 (Fonte: oaDOI API)
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