Noonan syndrome in diverse populations (2017)
- Authors:
- Kruszka, Paul
- Porras, Antonio R.
- Addissie, Yonit A.
- Moresco, Angélica
- Medrano, Sofia
- Mok, Gary T. K.
- Leung, Gordon K. C.
- Tekendo-Ngongang, Cedrik
- Uwineza, Annette
- Thong, Meow-Keong
- Muthukumarasamy, Premala
- Honey, Engela
- Ekure, Ekanem N.
- Sokunbi, Ogochukwu J.
- Kalu, Nnenna
- Jones, Kelly L.
- Kaplan, Julie D.
- Abdul-Rahman, Omar A.
- Vincent, Lisa M.
- Love, Amber
- Belhassan, Khadija
- Ouldim, Karim
- El Bouchikhi, Ihssane
- Shukla, Anju
- Girisha, Katta M.
- Patil, Siddaramappa J.
- Sirisena, Nirmala D.
- Dissanayake, Vajira H. W.
- Paththinige, C. Sampath
- Mishra, Rupesh
- Klein-Zighelboim, Eva
- Jugo, Bertha E. Gallardo
- Pastor, Miguel Chávez
- Abarca-Barriga, Hugo H.
- Skinner, Steven A.
- Prijoles, Eloise J.
- Badoe, Eben
- Gill, Ashleigh D.
- Shotelersuk, Vorasuk
- Smpokou, Patroula
- Kisling, Monisha S.
- Ferreira, Carlos R.
- Mutesa, Leon
- Megarbane, Andre
- Kline, Antonie D.
- Kimball, Amy
- Okello, Emmy
- Lwabi, Peter
- Aliku, Twalib
- Tenywa, Emmanuel
- Boonchooduang, Nonglak
- Tanpaiboon, Pranoot
- Richieri-Costa, Antonio
- Wonkam, Ambroise
- Chung, Brian H. Y.
- Stevenson, Roger E.
- Summar, Marshall
- Mandal, Kausik
- Phadke, Shubha R.
- Obregon, María G.
- Linguraru, Marius G.
- Muenke, Maximilian
- Autor USP: COSTA, ANTONIO RICHIERI DA - HRAC
- Unidade: HRAC
- DOI: 10.1002/ajmg.a.38362
- Subjects: SÍNDROME DE NOONAN; DELEÇÃO DE GENES; FENÓTIPOS; ANÁLISE FACIAL
- Language: Inglês
- Imprenta:
- Source:
- Título: American Journal of Medical Genetics. Part A
- ISSN: 1552-4825
- Volume/Número/Paginação/Ano: v. 173, n. 9, p. 2323-2334, Sept. 2017
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
KRUSZKA, Paul et al. Noonan syndrome in diverse populations. American Journal of Medical Genetics. Part A, v. 173, n. 9, p. 2323-2334, 2017Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.38362/epdf. Acesso em: 05 mar. 2026. -
APA
Kruszka, P., Porras, A. R., Addissie, Y. A., Moresco, A., Medrano, S., Mok, G. T. K., et al. (2017). Noonan syndrome in diverse populations. American Journal of Medical Genetics. Part A, 173( 9), 2323-2334. doi:10.1002/ajmg.a.38362 -
NLM
Kruszka P, Porras AR, Addissie YA, Moresco A, Medrano S, Mok GTK, Leung GKC, Tekendo-Ngongang C, Uwineza A, Thong M-K, Muthukumarasamy P, Honey E, Ekure EN, Sokunbi OJ, Kalu N, Jones KL, Kaplan JD, Abdul-Rahman OA, Vincent LM, Love A, Belhassan K, Ouldim K, El Bouchikhi I, Shukla A, Girisha KM, Patil SJ, Sirisena ND, Dissanayake VHW, Paththinige CS, Mishra R, Klein-Zighelboim E, Jugo BEG, Pastor MC, Abarca-Barriga HH, Skinner SA, Prijoles EJ, Badoe E, Gill AD, Shotelersuk V, Smpokou P, Kisling MS, Ferreira CR, Mutesa L, Megarbane A, Kline AD, Kimball A, Okello E, Lwabi P, Aliku T, Tenywa E, Boonchooduang N, Tanpaiboon P, Richieri-Costa A, Wonkam A, Chung BHY, Stevenson RE, Summar M, Mandal K, Phadke SR, Obregon MG, Linguraru MG, Muenke M. Noonan syndrome in diverse populations [Internet]. American Journal of Medical Genetics. Part A. 2017 ; 173( 9): 2323-2334.[citado 2026 mar. 05 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.38362/epdf -
Vancouver
Kruszka P, Porras AR, Addissie YA, Moresco A, Medrano S, Mok GTK, Leung GKC, Tekendo-Ngongang C, Uwineza A, Thong M-K, Muthukumarasamy P, Honey E, Ekure EN, Sokunbi OJ, Kalu N, Jones KL, Kaplan JD, Abdul-Rahman OA, Vincent LM, Love A, Belhassan K, Ouldim K, El Bouchikhi I, Shukla A, Girisha KM, Patil SJ, Sirisena ND, Dissanayake VHW, Paththinige CS, Mishra R, Klein-Zighelboim E, Jugo BEG, Pastor MC, Abarca-Barriga HH, Skinner SA, Prijoles EJ, Badoe E, Gill AD, Shotelersuk V, Smpokou P, Kisling MS, Ferreira CR, Mutesa L, Megarbane A, Kline AD, Kimball A, Okello E, Lwabi P, Aliku T, Tenywa E, Boonchooduang N, Tanpaiboon P, Richieri-Costa A, Wonkam A, Chung BHY, Stevenson RE, Summar M, Mandal K, Phadke SR, Obregon MG, Linguraru MG, Muenke M. Noonan syndrome in diverse populations [Internet]. American Journal of Medical Genetics. Part A. 2017 ; 173( 9): 2323-2334.[citado 2026 mar. 05 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.38362/epdf - Macrostomia, preauricular tags, and external ophthalmoplegia: a new autosomal dominant syndrome within the oculoauriculovertebral spectrum?
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Informações sobre o DOI: 10.1002/ajmg.a.38362 (Fonte: oaDOI API)
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