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Year | Number of Results |
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2009 | 1 |
2023 | 2 |
2024 | 2 |
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Page 1
Low-pass whole genome sequencing is a reliable and cost-effective approach for copy number variant analysis in the clinical setting.
Ann Hum Genet. 2024 Mar;88(2):113-125. doi: 10.1111/ahg.12532. Epub 2023 Oct 9.
Ann Hum Genet. 2024.
PMID: 37807935
[Hereditary tylosis syndrome and esophagus cancer].
de Souza CA, Santos Ada C, Santos Lda C, Carneiro AL.
de Souza CA, et al.
An Bras Dermatol. 2009 Sep-Oct;84(5):527-9. doi: 10.1590/s0365-05962009000500014.
An Bras Dermatol. 2009.
PMID: 20098858
Portuguese.
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Whole genome sequencing as a first-tier diagnostic test for infants in neonatal intensive care units: A pilot study in Brazil.
Migliavacca MP, Sobreira J, Bermeo D, Gomes M, Alencar D, Sussuchi L, Souza CA, Silva JS, Kroll JE, Burger M, Guarischi-Sousa R, Villela D, Yamamoto GL, Milanezi F, Horigoshi N, Cesar RG, de Carvalho WB, Honjo RS, Bertola DR, Kim CA, de Souza L, Procianoy RS, Silveria RC, Rosenberg C, Giugliani R, Campana GA, Scapulatempo-Neto C, Sobreira N.
Migliavacca MP, et al. Among authors: souza ca.
Am J Med Genet A. 2024 Jun;194(6):e63544. doi: 10.1002/ajmg.a.63544. Epub 2024 Jan 23.
Am J Med Genet A. 2024.
PMID: 38258498
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A Benchmark of In-House Homologous Recombination Repair Deficiency Testing Solutions for High-Grade Serous Ovarian Cancer Diagnosis.
Guarischi-Sousa R, Kroll JE, Bonaldi A, Pierry PM, Villela D, Souza CA, Silva JS, Bürger MC, Oliveira FA, de Paula MG, Meliso FM, de Almeida LG, Monfredini PM, de Oliveira AG, Milanezi F, Scapulatempo-Neto C, Yamamoto GL.
Guarischi-Sousa R, et al. Among authors: souza ca.
Diagnostics (Basel). 2023 Oct 24;13(21):3293. doi: 10.3390/diagnostics13213293.
Diagnostics (Basel). 2023.
PMID: 37958189
Free PMC article.
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