Artigo de periodico

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:
  • Publisher place: Hoboken
  • Date published: 2017
• Source:
  • Título: American Journal of Medical Genetics. Part A
  • Volume/Número/Paginação/Ano: v. 173, n. 4, p. 879-888, Feb. 2017


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• 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: 06 maio 2026.

• 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 2026 maio 06 ] 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 2026 maio 06 ] Available from: https://doi.org/10.1002/ajmg.a.38199

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