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 (2015)
- Authors:
- USP affiliated authors: SQUIRE, JEREMY ANDREW - FMRP ; MARTELLI, LUCIA REGINA - FMRP
- Unidade: FMRP
- Subjects: ANORMALIDADES CRANIOFACIAIS; ANORMALIDADES CROMOSSÔMICAS
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Resumos
- Conference titles: Reunião Brasileira de Citogenética
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ABNT
GRZESIUK, J. D. et al. 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. 2015, Anais.. Atibaia: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2015. . Acesso em: 26 abr. 2024. -
APA
Grzesiuk, J. D., Gomes, A. G., Grangeiro, C. H. P., Laureano, L. A. F., Huber, J., Squire, J. A., & Martelli, L. R. (2015). 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. In Resumos. Atibaia: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Grzesiuk JD, Gomes AG, Grangeiro CHP, Laureano LAF, Huber J, Squire JA, Martelli LR. 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. Resumos. 2015 ;[citado 2024 abr. 26 ] -
Vancouver
Grzesiuk JD, Gomes AG, Grangeiro CHP, Laureano LAF, Huber J, Squire JA, Martelli LR. 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. Resumos. 2015 ;[citado 2024 abr. 26 ] - Phenotype-genotype correlative characterization a case of Jacobsen Syndrome without thrombocytopenia associated with a ring chromosome 11
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- 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
- Karyotypy-phenotype-genotype correlation in a 4p;12q rearrangement
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