Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses (2021)
- Authors:
- Villela, Darine

- Mazzonetto, Patricia Camacho

- Migliavacca, Michele P
- Perrone, Eduardo
- Guida, Gustavo
- Milanezi, Maria Fernanda G
- Jorge, Alexander A. L

- Ribeiro-Bicudo, Lucilene A

- Kok, Fernando

- Campagnari, Francine
- Rosso-Giuliani, Liane de
- Costa, Silvia Souza da
- Vianna-Morgante, Angela M

- Pearson, Peter L
- Krepischi, Ana Cristina Victorino

- Rosenberg, Carla

- Villela, Darine
- USP affiliated authors: JORGE, ALEXANDER AUGUSTO DE LIMA - FM ; KOK, FERNANDO - FM ; COSTA, SILVIA SOUZA DA - IB ; MORGANTE, ANGELA MARIA VIANNA - IB ; PEARSON, PETER LEES - IB ; KREPISCHI, ANA CRISTINA VICTORINO - IB ; ROSENBERG, CARLA - IB ; VILLELA, DARINE CHRISTINA MAIA - IB
- Unidades: FM; IB
- DOI: 10.1002/ajmg.a.62237
- Subjects: DOENÇAS GENÉTICAS; DOENÇAS CONGÊNITAS; ANORMALIDADES CROMOSSÔMICAS; TRANSTORNO AUTÍSTICO
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título: American Journal of Medical Genetics. Part A
- ISSN: 1552-4833
- Volume/Número/Paginação/Ano: v. 185, n. 8, p. 2335-2344, 2021
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
VILLELA, Darine et al. Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses. American Journal of Medical Genetics. Part A, v. 185, n. 8, p. 2335-2344, 2021Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.62237. Acesso em: 28 dez. 2025. -
APA
Villela, D., Mazzonetto, P. C., Migliavacca, M. P., Perrone, E., Guida, G., Milanezi, M. F. G., et al. (2021). Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses. American Journal of Medical Genetics. Part A, 185( 8), 2335-2344. doi:10.1002/ajmg.a.62237 -
NLM
Villela D, Mazzonetto PC, Migliavacca MP, Perrone E, Guida G, Milanezi MFG, Jorge AAL, Ribeiro-Bicudo LA, Kok F, Campagnari F, Rosso-Giuliani L de, Costa SS da, Vianna-Morgante AM, Pearson PL, Krepischi ACV, Rosenberg C. Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses [Internet]. American Journal of Medical Genetics. Part A. 2021 ; 185( 8): 2335-2344.[citado 2025 dez. 28 ] Available from: https://doi.org/10.1002/ajmg.a.62237 -
Vancouver
Villela D, Mazzonetto PC, Migliavacca MP, Perrone E, Guida G, Milanezi MFG, Jorge AAL, Ribeiro-Bicudo LA, Kok F, Campagnari F, Rosso-Giuliani L de, Costa SS da, Vianna-Morgante AM, Pearson PL, Krepischi ACV, Rosenberg C. Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses [Internet]. American Journal of Medical Genetics. Part A. 2021 ; 185( 8): 2335-2344.[citado 2025 dez. 28 ] Available from: https://doi.org/10.1002/ajmg.a.62237 - Chromosomal microarray analyses from 5778 patients with neurodevelopmental disorders and congenital anomalies in Brazil
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- X-chromosome microimbalances in boys with intellectual disability and maternal completely skewed X-inactivation
- Germline copy number variations and cancer predisposition
- Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways
- Mechanistic insights revealed by a UBE2A mutation linked to intellectual disability
Informações sobre o DOI: 10.1002/ajmg.a.62237 (Fonte: oaDOI API)
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