Identification of a rare copy number polymorphic gain at 3q12.2 with candidate genes for familial endometriosis (2024)
- Authors:
- USP affiliated authors: SILVA, JULIO CESAR ROSA E - FMRP ; SQUIRE, JEREMY ANDREW - FMRP ; PANEPUCCI, RODRIGO ALEXANDRE - FMRP ; LOVATO, JULIANA MEOLA - FMRP ; MARTELLI, LUCIA REGINA - FMRP
- Unidade: FMRP
- DOI: 10.61622/rbgo/2024CR12
- Subjects: GENES; ENDOMETRIOSE; POLIMORFISMO
- Keywords: Endometriosis; Endometrium; Heredity; Array-CGH; Genomic structural variation; DNA copy number variations; Polymorphism; Genetic
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Publisher place: Rio de Janeiro
- Date published: 2024
- Source:
- Título: Revista Brasileira de Ginecologia e Obstetrícia
- ISSN: 0100-7203
- Volume/Número/Paginação/Ano: v. 46, p. 1-6, 2024
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
OLIVEIRA, Flávia Gaona et al. Identification of a rare copy number polymorphic gain at 3q12.2 with candidate genes for familial endometriosis. Revista Brasileira de Ginecologia e Obstetrícia, v. 46, p. 1-6, 2024Tradução . . Disponível em: https://doi.org/10.61622/rbgo/2024CR12. Acesso em: 19 fev. 2026. -
APA
Oliveira, F. G., Silva, J. C. R. e, Gomes, A. G., Grzesiuk, J. D., Vidotto, T., Squire, J. A., et al. (2024). Identification of a rare copy number polymorphic gain at 3q12.2 with candidate genes for familial endometriosis. Revista Brasileira de Ginecologia e Obstetrícia, 46, 1-6. doi:10.61622/rbgo/2024CR12 -
NLM
Oliveira FG, Silva JCR e, Gomes AG, Grzesiuk JD, Vidotto T, Squire JA, Panepucci RA, Meola J, Martelli LR. Identification of a rare copy number polymorphic gain at 3q12.2 with candidate genes for familial endometriosis [Internet]. Revista Brasileira de Ginecologia e Obstetrícia. 2024 ; 46 1-6.[citado 2026 fev. 19 ] Available from: https://doi.org/10.61622/rbgo/2024CR12 -
Vancouver
Oliveira FG, Silva JCR e, Gomes AG, Grzesiuk JD, Vidotto T, Squire JA, Panepucci RA, Meola J, Martelli LR. Identification of a rare copy number polymorphic gain at 3q12.2 with candidate genes for familial endometriosis [Internet]. Revista Brasileira de Ginecologia e Obstetrícia. 2024 ; 46 1-6.[citado 2026 fev. 19 ] Available from: https://doi.org/10.61622/rbgo/2024CR12 - Etiopatogenia: teorias contemporâneas
- Applications of cytogenomic characterization of chromosomal rearrangements to establish a more precise phenotype-genotype correlation
- Chromosomal gain at an unstable region of 15q11.2 in a family with intellectual disability and behavioral disorder
- Analysis of complex duplication-deletion (8p) rearrangement: clinical, cytogenetic and array comparative genomic characterization
- High resolution array-CGH analysis apparently balanced translocations reveals complex chromosomal rearrangement and cryptic deletions associated with the phenotypes
- Chromosomal gain at an unstable region of 15q11.2 in a family with intellectual disability and behavioral disorder
- Genotype-phenotype correlation of an 8p complex rearrangement
- High resolution mapping of 12p in a patient with a mild phenotype of Pallister-Killian syndrome indicates duplication by interstitial gain of 12p11.21-p13.31
- Genotype-phenotype correlation associated with inherited homozygous paracentric inversion of chromosome 12
- High resolution array-CGH analysis of apparently balanced translocations reveals complex chromosomal rearrangement and cryptic deletions associated with the phenotypes
Informações sobre o DOI: 10.61622/rbgo/2024CR12 (Fonte: oaDOI API)
Download do texto completo
| Tipo | Nome | Link | |
|---|---|---|---|
 |
003203589.pdf | Direct link |
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
