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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
Source: American Journal of Medical Genetics. Part A. Unidade: HRAC
Subjects: ANÁLISE FACIAL, FENÓTIPOS, ANÁLISE FACIAL
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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: 12 nov. 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 nov. 12 ] 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 nov. 12 ] Available from: https://doi.org/10.1002/ajmg.a.38199
Artigo de periodico
Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes (2002)
Kondo, Shinji; Schutte, Brian C.; Richardson, Rebecca J.; Bjork, Bryan C.; Knight, Alexandra S.; Watanabe, Yoriko; Howard, Emma; Lima, Renata L. L. Ferreira de; Hirsch, Sandra Daack; Sander, Achim; McGinn, Donna M. McDonald; Zackai, Elaine H.; Lammer, Edward J; Aylsworth, Arthur S.; Ardinger, Holly H.; Lidral, Andrew C.; Pober, Barbara R.; Moreno, Lina; Burgos, Mauricio Arcos; Valencia, Consuelo; Houdayer, Claude; Bahuau, Michel; Moretti Ferreira, Danilo; Richieri-Costa, Antonio; Dixon, Michael J.; Murray, Jeffrey C.
Source: Nature Genetics. Unidade: HRAC
Assunto: SÍNDROMES OROFACIODIGITAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KONDO, Shinji et al. Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes. Nature Genetics, v. 32, n. 2, p. 285-289, 2002Tradução . . Disponível em: https://doi.org/10.1038/ng985. Acesso em: 12 nov. 2024.
APA
Kondo, S., Schutte, B. C., Richardson, R. J., Bjork, B. C., Knight, A. S., Watanabe, Y., et al. (2002). Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes. Nature Genetics, 32( 2), 285-289. doi:10.1038/ng985
NLM
Kondo S, Schutte BC, Richardson RJ, Bjork BC, Knight AS, Watanabe Y, Howard E, Lima RLLF de, Hirsch SD, Sander A, McGinn DMMD, Zackai EH, Lammer EJ, Aylsworth AS, Ardinger HH, Lidral AC, Pober BR, Moreno L, Burgos MA, Valencia C, Houdayer C, Bahuau M, Moretti Ferreira D, Richieri-Costa A, Dixon MJ, Murray JC. Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes [Internet]. Nature Genetics. 2002 ; 32( 2): 285-289.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1038/ng985
Vancouver
Kondo S, Schutte BC, Richardson RJ, Bjork BC, Knight AS, Watanabe Y, Howard E, Lima RLLF de, Hirsch SD, Sander A, McGinn DMMD, Zackai EH, Lammer EJ, Aylsworth AS, Ardinger HH, Lidral AC, Pober BR, Moreno L, Burgos MA, Valencia C, Houdayer C, Bahuau M, Moretti Ferreira D, Richieri-Costa A, Dixon MJ, Murray JC. Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes [Internet]. Nature Genetics. 2002 ; 32( 2): 285-289.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1038/ng985
Artigo de periodico
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly (1999)
Wallis, Deeann E.; Roessler, Erich; Hehr, Ute; Nanni, Luisa; Wiltshire, Tim; Richieri-Costa, Antonio; Gillessen-Kaesbach, Gabriele; Zackai, Elaine H.; Rommens, Johanna; Muenke, Maximilian
Source: Nature Genetics. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
WALLIS, Deeann E. et al. Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly. Nature Genetics, v. 22, n. 2, p. 196-198, 1999Tradução . . Disponível em: https://doi.org/10.1038/9718. Acesso em: 12 nov. 2024.
APA
Wallis, D. E., Roessler, E., Hehr, U., Nanni, L., Wiltshire, T., Richieri-Costa, A., et al. (1999). Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly. Nature Genetics, 22( 2), 196-198. doi:10.1038/9718
NLM
Wallis DE, Roessler E, Hehr U, Nanni L, Wiltshire T, Richieri-Costa A, Gillessen-Kaesbach G, Zackai EH, Rommens J, Muenke M. Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly [Internet]. Nature Genetics. 1999 ; 22( 2): 196-198.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1038/9718
Vancouver
Wallis DE, Roessler E, Hehr U, Nanni L, Wiltshire T, Richieri-Costa A, Gillessen-Kaesbach G, Zackai EH, Rommens J, Muenke M. Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly [Internet]. Nature Genetics. 1999 ; 22( 2): 196-198.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1038/9718

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