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Milena Simioni

Showing results (11-20 of 25) with videos related to

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European Journal of Medical Genetics|July 27, 2013
Atypical copy number abnormalities in 22q11.2 region: report of three casesMiriam Coelho Molck, Társis Paiva Vieira, Ilária Cristina Sgardioli, et al.
Molecular Syndromology|July 11, 2017
Genomic Investigation of Balanced Chromosomal Rearrangements in Patients with Abnormal PhenotypesMilena Simioni, François Artiguenave, Vincent Meyer, et al.
American Journal of Medical Genetics. Part A|September 20, 2012
Insertional translocation of 15q25-q26 into 11p13 and duplication at 8p23.1 characterized by high resolution arrays in a boy with congenital malformations and aniridiaMilena Simioni, Társis Paiva Vieira, Ilária Cristina Sgardioli, et al.
European Journal of Medical Genetics|July 24, 2012
A familial case with interstitial 2q36 deletion: variable phenotypic expression in full and mosaic stateÉrika L Freitas, Susan M Gribble, Milena Simioni, et al.
Annals of Human Genetics|September 13, 2017
Ancestry Informative Marker Panel to Estimate Population Stratification Using Genome-wide Human ArrayFernanda B Barbosa, Natalia F Cagnin, Milena Simioni, et al.
Jornal De Pediatria|March 25, 2017
Genomic imbalances in syndromic congenital heart diseaseMiriam Coelho Molck, Milena Simioni, Társis Paiva Vieira, et al.
Plos One|November 29, 2018
Copy number variation in the susceptibility to systemic lupus erythematosusFernanda Bueno Barbosa, Milena Simioni, Cláudia Emília Vieira Wiezel, et al.
Scientific Reports|July 28, 2019
Genetic comparison of sickle cell anaemia cohorts from Brazil and the United States reveals high levels of divergencePedro R S Cruz, Galina Ananina, Vera Lucia Gil-da-Silva-Lopes, et al.
American Journal of Medical Genetics. Part A|December 8, 2015
Genotype-phenotype correlation of 16p13.3 terminal duplication and 22q13.33 deletion: Natural history of a patient and review of the literatureMarshall I B Fontes, Ana P Santos, Miriam C Molck, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|March 24, 2016
A Cytogenomic Approach in a Case of Syndromic XY Gonadal DysgenesisMilena Simioni, Isabella Lopes Monlleó, Camila M Costa de Queiroz, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
European Journal of Medical Genetics|July 27, 2013
Atypical copy number abnormalities in 22q11.2 region: report of three casesMiriam Coelho Molck, Társis Paiva Vieira, Ilária Cristina Sgardioli, et al.
Molecular Syndromology|July 11, 2017
Genomic Investigation of Balanced Chromosomal Rearrangements in Patients with Abnormal PhenotypesMilena Simioni, François Artiguenave, Vincent Meyer, et al.
American Journal of Medical Genetics. Part A|September 20, 2012
Insertional translocation of 15q25-q26 into 11p13 and duplication at 8p23.1 characterized by high resolution arrays in a boy with congenital malformations and aniridiaMilena Simioni, Társis Paiva Vieira, Ilária Cristina Sgardioli, et al.
European Journal of Medical Genetics|July 24, 2012
A familial case with interstitial 2q36 deletion: variable phenotypic expression in full and mosaic stateÉrika L Freitas, Susan M Gribble, Milena Simioni, et al.
Annals of Human Genetics|September 13, 2017
Ancestry Informative Marker Panel to Estimate Population Stratification Using Genome-wide Human ArrayFernanda B Barbosa, Natalia F Cagnin, Milena Simioni, et al.
Jornal De Pediatria|March 25, 2017
Genomic imbalances in syndromic congenital heart diseaseMiriam Coelho Molck, Milena Simioni, Társis Paiva Vieira, et al.
Plos One|November 29, 2018
Copy number variation in the susceptibility to systemic lupus erythematosusFernanda Bueno Barbosa, Milena Simioni, Cláudia Emília Vieira Wiezel, et al.
Scientific Reports|July 28, 2019
Genetic comparison of sickle cell anaemia cohorts from Brazil and the United States reveals high levels of divergencePedro R S Cruz, Galina Ananina, Vera Lucia Gil-da-Silva-Lopes, et al.
American Journal of Medical Genetics. Part A|December 8, 2015
Genotype-phenotype correlation of 16p13.3 terminal duplication and 22q13.33 deletion: Natural history of a patient and review of the literatureMarshall I B Fontes, Ana P Santos, Miriam C Molck, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|March 24, 2016
A Cytogenomic Approach in a Case of Syndromic XY Gonadal DysgenesisMilena Simioni, Isabella Lopes Monlleó, Camila M Costa de Queiroz, et al.
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