Partial monosomy 4p and trisomy 12q due to a t(4;12)(p16.3;q24.31) familial translocation in two cousins (2019)
- Authors:
- USP affiliated authors: SQUIRE, JEREMY ANDREW - FMRP ; MARTELLI, LUCIA REGINA - FMRP ; GRANGEIRO, CARLOS HENRIQUE PAIVA - FMRP ; GENNARO, FLAVIA GAONA DE OLIVEIRA - FMRP ; GOMES, ALEXANDRA GALVÃO - FMRP
- Unidade: FMRP
- DOI: 10.1159/000501923
- Subjects: GENÔMICA; GENÓTIPOS; FENÓTIPOS; CROMOSSOMOS; HIBRIDIZAÇÃO; MALFORMAÇÕES; DELEÇÃO DE GENES
- Keywords: Chromosomal translocation; Comparative genomic hybridization; Genotype-phenotype association; Partial monosomy 4p16; Partial trisomy 12q; Wolf-Hirschhorn syndrome
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Molecular Syndromology
- ISSN: 1661-8769
- Volume/Número/Paginação/Ano: v. 10, n. 5, p. 264-271, 2019
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: bronze
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ABNT
JOAQUIM, Tatiana Mozer et al. Partial monosomy 4p and trisomy 12q due to a t(4;12)(p16.3;q24.31) familial translocation in two cousins. Molecular Syndromology, v. 10, n. 5, p. 264-271, 2019Tradução . . Disponível em: https://doi.org/10.1159/000501923. Acesso em: 15 maio 2024. -
APA
Joaquim, T. M., Grangeiro, C. H. P., Gennaro, F. G. de O., Gomes, A. G., Squire, J. A., & Martelli, L. R. (2019). Partial monosomy 4p and trisomy 12q due to a t(4;12)(p16.3;q24.31) familial translocation in two cousins. Molecular Syndromology, 10( 5), 264-271. doi:10.1159/000501923 -
NLM
Joaquim TM, Grangeiro CHP, Gennaro FG de O, Gomes AG, Squire JA, Martelli LR. Partial monosomy 4p and trisomy 12q due to a t(4;12)(p16.3;q24.31) familial translocation in two cousins [Internet]. Molecular Syndromology. 2019 ; 10( 5): 264-271.[citado 2024 maio 15 ] Available from: https://doi.org/10.1159/000501923 -
Vancouver
Joaquim TM, Grangeiro CHP, Gennaro FG de O, Gomes AG, Squire JA, Martelli LR. Partial monosomy 4p and trisomy 12q due to a t(4;12)(p16.3;q24.31) familial translocation in two cousins [Internet]. Molecular Syndromology. 2019 ; 10( 5): 264-271.[citado 2024 maio 15 ] Available from: https://doi.org/10.1159/000501923 - Phenotype-genotype correlative characterization a case of Jacobsen Syndrome without thrombocytopenia associated with a ring chromosome 11
- 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
- Familial non-disjunction and segregation variation of a supernumerary marker chromosome 15 in members of a large family
- Phenotype-genotype correlative characterization a case of Jacobsen Syndrome associated with a ring chromosome 11
- Genotype-phenotype correlation with ring chromosome 11
- Genotype-phenotype correlation associated with inherited homozygous paracentric inversion of chromosome 12
- Karyotype-phenotype-genotype correlation in a 4p;12q rearrangement
- Complex mosaic ring chromosome 11 associated with hemizygous loss of 8.6 Mb of 11q24.2qter in atypical Jacobsen syndrome
- Chromosomal gain at an unstable region of 15q11.2 in a family with intellectual disability and behavioral disorder
Informações sobre o DOI: 10.1159/000501923 (Fonte: oaDOI API)
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