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Israel Gomy

Showing results (11-20 of 28) with videos related to

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European Radiology|July 29, 2024
Baseline surveillance in Li Fraumeni syndrome using whole-body MRI: a systematic review and updated meta-analysisMaria Inez Dacoregio, Pedro Cotta Abrahão Reis, Davi Said Gonçalves Celso, et al.
Familial Cancer|June 23, 2010
Clinical and molecular characterization of Brazilian families with von Hippel-Lindau disease: a need for delineating genotype-phenotype correlationIsrael Gomy, Greice Andreotti Molfetta, Ester de Andrade Barreto, et al.
American Journal of Medical Genetics. Part A|January 31, 2014
Mucopolysaccharidosis type IVA: evidence of primary and secondary central nervous system involvementFelippe Borlot, Paula Ricci Arantes, Caio Robledo Quaio, et al.
International Journal of Cancer|December 2, 2015
Contribution of rare germline copy number variations and common susceptibility loci in Lynch syndrome patients negative for mutations in the mismatch repair genesRolando A R Villacis, Priscila M Miranda, Israel Gomy, et al.
Clinics (Sao Paulo, Brazil)|September 6, 2012
A clinical follow-up of 35 Brazilian patients with Prader-Willi syndromeCaio Robledo D'Angioli Costa Quaio, Tatiana Ferreira de Almeida, Lilian Maria José Albano, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|July 17, 2004
Splenopancreatic field abnormality is not unique to trisomy 13Luiz Cesar Peres, Gustavo Henrique T de Sales Barbosa, Renata Scarpat Careta, et al.
Movement Disorders Clinical Practice|April 10, 2026
Epileptic-Dyskinetic Encephalopathy Associated with a PPP3CA Variant: Expansion of the Phenotypic SpectrumBruno Antunes Contrucci, Ursula Thomé, Larissa Aparecida Batista, et al.
BMC Cancer|February 11, 2012
Predictive models for mutations in mismatch repair genes: implication for genetic counseling in developing countriesErika Maria Monteiro Santos, Mev Dominguez Valentin, Felipe Carneiro, et al.
American Journal of Medical Genetics. Part A|December 31, 2020
Clinical and molecular evaluation of 13 Brazilian patients with Gomez-López-Hernández syndromeEduardo Perrone, Ana Beatriz Alvarez Perez, Vânia D'Almeida, et al.
Anticancer Research|October 13, 2012
Evaluation of MLH1 I219V polymorphism in unrelated South American individuals suspected of having Lynch syndromeMev Dominguez Valentin, Felipe Carneiro Da Silva, Erika Maria Monteiro Santos, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
European Radiology|July 29, 2024
Baseline surveillance in Li Fraumeni syndrome using whole-body MRI: a systematic review and updated meta-analysisMaria Inez Dacoregio, Pedro Cotta Abrahão Reis, Davi Said Gonçalves Celso, et al.
Familial Cancer|June 23, 2010
Clinical and molecular characterization of Brazilian families with von Hippel-Lindau disease: a need for delineating genotype-phenotype correlationIsrael Gomy, Greice Andreotti Molfetta, Ester de Andrade Barreto, et al.
American Journal of Medical Genetics. Part A|January 31, 2014
Mucopolysaccharidosis type IVA: evidence of primary and secondary central nervous system involvementFelippe Borlot, Paula Ricci Arantes, Caio Robledo Quaio, et al.
International Journal of Cancer|December 2, 2015
Contribution of rare germline copy number variations and common susceptibility loci in Lynch syndrome patients negative for mutations in the mismatch repair genesRolando A R Villacis, Priscila M Miranda, Israel Gomy, et al.
Clinics (Sao Paulo, Brazil)|September 6, 2012
A clinical follow-up of 35 Brazilian patients with Prader-Willi syndromeCaio Robledo D'Angioli Costa Quaio, Tatiana Ferreira de Almeida, Lilian Maria José Albano, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|July 17, 2004
Splenopancreatic field abnormality is not unique to trisomy 13Luiz Cesar Peres, Gustavo Henrique T de Sales Barbosa, Renata Scarpat Careta, et al.
Movement Disorders Clinical Practice|April 10, 2026
Epileptic-Dyskinetic Encephalopathy Associated with a PPP3CA Variant: Expansion of the Phenotypic SpectrumBruno Antunes Contrucci, Ursula Thomé, Larissa Aparecida Batista, et al.
BMC Cancer|February 11, 2012
Predictive models for mutations in mismatch repair genes: implication for genetic counseling in developing countriesErika Maria Monteiro Santos, Mev Dominguez Valentin, Felipe Carneiro, et al.
American Journal of Medical Genetics. Part A|December 31, 2020
Clinical and molecular evaluation of 13 Brazilian patients with Gomez-López-Hernández syndromeEduardo Perrone, Ana Beatriz Alvarez Perez, Vânia D'Almeida, et al.
Anticancer Research|October 13, 2012
Evaluation of MLH1 I219V polymorphism in unrelated South American individuals suspected of having Lynch syndromeMev Dominguez Valentin, Felipe Carneiro Da Silva, Erika Maria Monteiro Santos, et al.
Pageof 3