| Case Report Online Published: 10 Oct 2021 | ||||||||||||
Cornelia de Lange syndrome - rare mutation of SMC1A gene Lídia Leite, Vasco Carvalho, Miguel Rocha, Almerinda Barroso Pereira, Liliana Pinheiro.
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| How to Cite this Article |
| Pubmed Style Leite L, Carvalho V, Rocha M, Pereira AB, Pinheiro L. Cornelia de Lange syndrome - rare mutation of SMC1A gene. Int J Med Rev Case Rep. 2021; 5(9): 73-75. doi:10.5455/IJMRCR.Cornelia-de-Lange-syndrome Web Style Leite L, Carvalho V, Rocha M, Pereira AB, Pinheiro L. Cornelia de Lange syndrome - rare mutation of SMC1A gene. https://www.mdpub.net/?mno=109122 [Access: October 13, 2024]. doi:10.5455/IJMRCR.Cornelia-de-Lange-syndrome AMA (American Medical Association) Style Leite L, Carvalho V, Rocha M, Pereira AB, Pinheiro L. Cornelia de Lange syndrome - rare mutation of SMC1A gene. Int J Med Rev Case Rep. 2021; 5(9): 73-75. doi:10.5455/IJMRCR.Cornelia-de-Lange-syndrome Vancouver/ICMJE Style Leite L, Carvalho V, Rocha M, Pereira AB, Pinheiro L. Cornelia de Lange syndrome - rare mutation of SMC1A gene. Int J Med Rev Case Rep. (2021), [cited October 13, 2024]; 5(9): 73-75. doi:10.5455/IJMRCR.Cornelia-de-Lange-syndrome Harvard Style Leite, L., Carvalho, . V., Rocha, . M., Pereira, . A. B. & Pinheiro, . L. (2021) Cornelia de Lange syndrome - rare mutation of SMC1A gene. Int J Med Rev Case Rep, 5 (9), 73-75. doi:10.5455/IJMRCR.Cornelia-de-Lange-syndrome Turabian Style Leite, Lídia, Vasco Carvalho, Miguel Rocha, Almerinda Barroso Pereira, and Liliana Pinheiro. 2021. Cornelia de Lange syndrome - rare mutation of SMC1A gene. International Journal of Medical Reviews and Case Reports, 5 (9), 73-75. doi:10.5455/IJMRCR.Cornelia-de-Lange-syndrome Chicago Style Leite, Lídia, Vasco Carvalho, Miguel Rocha, Almerinda Barroso Pereira, and Liliana Pinheiro. "Cornelia de Lange syndrome - rare mutation of SMC1A gene." International Journal of Medical Reviews and Case Reports 5 (2021), 73-75. doi:10.5455/IJMRCR.Cornelia-de-Lange-syndrome MLA (The Modern Language Association) Style Leite, Lídia, Vasco Carvalho, Miguel Rocha, Almerinda Barroso Pereira, and Liliana Pinheiro. "Cornelia de Lange syndrome - rare mutation of SMC1A gene." International Journal of Medical Reviews and Case Reports 5.9 (2021), 73-75. Print. doi:10.5455/IJMRCR.Cornelia-de-Lange-syndrome APA (American Psychological Association) Style Leite, L., Carvalho, . V., Rocha, . M., Pereira, . A. B. & Pinheiro, . L. (2021) Cornelia de Lange syndrome - rare mutation of SMC1A gene. International Journal of Medical Reviews and Case Reports, 5 (9), 73-75. doi:10.5455/IJMRCR.Cornelia-de-Lange-syndrome |
