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: American Journal of Medical Genetics. Part A
- Volume/Número/Paginação/Ano: v. 173, n. 4, p. 879-888, Feb. 2017
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
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: 28 jan. 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 jan. 28 ] 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 jan. 28 ] Available from: https://doi.org/10.1002/ajmg.a.38199 - Autosomal recessive blepharoptosis, cleft lip/palate, dental anomalies, and ectrodactyly
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Informações sobre o DOI: 10.1002/ajmg.a.38199 (Fonte: oaDOI API)
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