Low-pass whole genome sequencing as a cost-effective alternative to chromosomal microarray analysis for low- and middle-income countries (2024)
- Authors:
- Mazzonetto, Patricia Camacho

- Villela, Darine

- Krepischi, Ana Cristina Victorino

- Pierry, Paulo Marques

- Bonaldi, Adriano
- Almeida, Luiz Gustavo Dufner de

- Paula, Marcelo Gomes de

- Bürger, Matheus Carvalho

- Oliveira, Ana Gabriela de
- Fonseca, Gustavo G. G
- Giugliani, Roberto

- Riegel-Giugliani, Mariluce

- Bertola, Débora Romeo

- Yamamoto, Guilherme Lopes

- Passos-Bueno, Maria Rita

- Campos, Gabriele da Silva

- Machado, Ana Claudia Dantas

- Mazzeu, Juliana Forte

- Perrone, Eduardo

- Zechi-Ceide, Roseli Maria

- Kokitsu-Nakata, Nancy Mizue

- Vieira, Társis Paiva

- Steiner, Carlos Eduardo

- Gil-da-Silva-Lopes, Vera Lúcia

- Vieira, Daniela Koeller Rodrigues
- Boy, Raquel

- Pina Neto, João Monteiro de

- Scapulatempo Neto, Cristovam

- Milanezi, Fernanda

- Rosenberg, Carla

- Mazzonetto, Patricia Camacho
- USP affiliated authors: KREPISCHI, ANA CRISTINA VICTORINO - IB ; BERTOLA, DÉBORA ROMEO - IB ; YAMAMOTO, GUILHERME LOPES - Interunidades em Bioinformática ; BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; CEIDE, ROSELI MARIA ZECHI - HRAC ; NAKATA, NANCY MIZUE KOKITSU - HRAC ; PINA NETO, JOÃO MONTEIRO DE - FMRP ; ROSENBERG, CARLA - IB ; MAZZONETTO, PATRICIA CAMACHO - IB ; CAMPOS, GABRIELE DA SILVA - IB ; MACHADO, ANA CLAUDIA DANTAS - IB
- Unidades: IB; Interunidades em Bioinformática; HRAC; FMRP
- DOI: 10.1002/ajmg.a.63802
- Subjects: CITOGENÉTICA; GENOMAS; CUIDADO PÓS-NATAL; DIAGNÓSTICO
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Publisher place: Hoboken, NJ
- Date published: 2024
- Source:
- Título: American Journal of Medical Genetics. Part A
- ISSN: 1552-4833
- Volume/Número/Paginação/Ano: v. 194, n. 11, p. e63802, Nov. 2024
- Status:
- Artigo possui acesso gratuito no site do editor (Bronze Open Access)
- Versão do Documento:
- Versão publicada (Published version)
- Acessar versão aberta:
-
ABNT
MAZZONETTO, Patricia Camacho et al. Low-pass whole genome sequencing as a cost-effective alternative to chromosomal microarray analysis for low- and middle-income countries. American Journal of Medical Genetics. Part A, v. No 2024, n. 11, p. e63802, 2024Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.63802. Acesso em: 06 maio 2026. -
APA
Mazzonetto, P. C., Villela, D., Krepischi, A. C. V., Pierry, P. M., Bonaldi, A., Almeida, L. G. D. de, et al. (2024). Low-pass whole genome sequencing as a cost-effective alternative to chromosomal microarray analysis for low- and middle-income countries. American Journal of Medical Genetics. Part A, No 2024( 11), e63802. doi:10.1002/ajmg.a.63802 -
NLM
Mazzonetto PC, Villela D, Krepischi ACV, Pierry PM, Bonaldi A, Almeida LGD de, Paula MG de, Bürger MC, Oliveira AG de, Fonseca GGG, Giugliani R, Riegel-Giugliani M, Bertola DR, Yamamoto GL, Passos-Bueno MR, Campos G da S, Machado ACD, Mazzeu JF, Perrone E, Zechi-Ceide RM, Kokitsu-Nakata NM, Vieira TP, Steiner CE, Gil-da-Silva-Lopes VL, Vieira DKR, Boy R, Pina Neto JM de, Scapulatempo Neto C, Milanezi F, Rosenberg C. Low-pass whole genome sequencing as a cost-effective alternative to chromosomal microarray analysis for low- and middle-income countries [Internet]. American Journal of Medical Genetics. Part A. 2024 ; No 2024( 11): e63802.[citado 2026 maio 06 ] Available from: https://doi.org/10.1002/ajmg.a.63802 -
Vancouver
Mazzonetto PC, Villela D, Krepischi ACV, Pierry PM, Bonaldi A, Almeida LGD de, Paula MG de, Bürger MC, Oliveira AG de, Fonseca GGG, Giugliani R, Riegel-Giugliani M, Bertola DR, Yamamoto GL, Passos-Bueno MR, Campos G da S, Machado ACD, Mazzeu JF, Perrone E, Zechi-Ceide RM, Kokitsu-Nakata NM, Vieira TP, Steiner CE, Gil-da-Silva-Lopes VL, Vieira DKR, Boy R, Pina Neto JM de, Scapulatempo Neto C, Milanezi F, Rosenberg C. Low-pass whole genome sequencing as a cost-effective alternative to chromosomal microarray analysis for low- and middle-income countries [Internet]. American Journal of Medical Genetics. Part A. 2024 ; No 2024( 11): e63802.[citado 2026 maio 06 ] Available from: https://doi.org/10.1002/ajmg.a.63802 - Clinical and cytogenetic impact of maternal balanced double translocation: a familial case of 15q11.2 microduplication and microdeletion syndromes with genetic counselling implications
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