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J Amor

Showing results (291-300 of 430) with videos related to

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Clinical Chemistry|December 31, 2015
Identification of Males with Cryptic Fragile X Alleles by Methylation-Specific Quantitative Melt AnalysisSolange M Aliaga, Howard R Slater, David Francis, et al.
European Journal of Human Genetics : EJHG|February 8, 2018
Offering pregnant women different levels of genetic information from prenatal chromosome microarray: a prospective studyJane L Halliday, Cecile Muller, Taryn Charles, et al.
Journal of Clinical Medicine|September 28, 2023
Bariatric Surgery Outcomes in Patients with Chronic Kidney DiseaseAdriana Pané, Maria Claro, Alicia Molina-Andujar, et al.
Human Mutation|August 19, 2011
Extending the scope of diagnostic chromosome analysis: detection of single gene defects using high-resolution SNP microarraysDamien L Bruno, Zornitza Stark, David J Amor, et al.
Diabetes Research and Clinical Practice|July 6, 2024
Dose-Dependent association of cumulative tobacco consumption with the presence of carotid atherosclerosis in individuals with type 1 diabetesClara Solà, Clara Viñals, Tonet Serés-Noriega, et al.
Epigenomics|October 4, 2024
Epigenomic newborn screening for conditions with intellectual disability and autistic features in Australian newbornsMohammed Alshawsh, Melissa Wake, Jozef Gecz, et al.
International Journal of Molecular Sciences|August 14, 2019
Significantly Elevated <i>FMR1</i> mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X TestingMichael Field, Tracy Dudding-Byth, Marta Arpone, et al.
Prenatal Diagnosis|December 25, 2025
Implementing Publicly Funded Fetal Exome Sequencing: A Statewide Multidisciplinary Model for Equitable Integration of Genomics Into Perinatal CareWillem Gheysen, Calder Hamill, Susan Fawcett, et al.
Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|February 28, 2022
Results of a multidisciplinary strategy to improve the management of cardiovascular risk factors after liver transplantationLydia Sastre, Raquel García, Clara Viñals, et al.
Journal of Medical Genetics|November 1, 2011
Pathogenic aberrations revealed exclusively by single nucleotide polymorphism (SNP) genotyping data in 5000 samples tested by molecular karyotypingD L Bruno, S M White, D Ganesamoorthy, et al.
Pageof 43

Showing results (291-300 of 430) with videos related to

Sort By:
Pageof 43
Clinical Chemistry|December 31, 2015
Identification of Males with Cryptic Fragile X Alleles by Methylation-Specific Quantitative Melt AnalysisSolange M Aliaga, Howard R Slater, David Francis, et al.
European Journal of Human Genetics : EJHG|February 8, 2018
Offering pregnant women different levels of genetic information from prenatal chromosome microarray: a prospective studyJane L Halliday, Cecile Muller, Taryn Charles, et al.
Journal of Clinical Medicine|September 28, 2023
Bariatric Surgery Outcomes in Patients with Chronic Kidney DiseaseAdriana Pané, Maria Claro, Alicia Molina-Andujar, et al.
Human Mutation|August 19, 2011
Extending the scope of diagnostic chromosome analysis: detection of single gene defects using high-resolution SNP microarraysDamien L Bruno, Zornitza Stark, David J Amor, et al.
Diabetes Research and Clinical Practice|July 6, 2024
Dose-Dependent association of cumulative tobacco consumption with the presence of carotid atherosclerosis in individuals with type 1 diabetesClara Solà, Clara Viñals, Tonet Serés-Noriega, et al.
Epigenomics|October 4, 2024
Epigenomic newborn screening for conditions with intellectual disability and autistic features in Australian newbornsMohammed Alshawsh, Melissa Wake, Jozef Gecz, et al.
International Journal of Molecular Sciences|August 14, 2019
Significantly Elevated <i>FMR1</i> mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X TestingMichael Field, Tracy Dudding-Byth, Marta Arpone, et al.
Prenatal Diagnosis|December 25, 2025
Implementing Publicly Funded Fetal Exome Sequencing: A Statewide Multidisciplinary Model for Equitable Integration of Genomics Into Perinatal CareWillem Gheysen, Calder Hamill, Susan Fawcett, et al.
Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|February 28, 2022
Results of a multidisciplinary strategy to improve the management of cardiovascular risk factors after liver transplantationLydia Sastre, Raquel García, Clara Viñals, et al.
Journal of Medical Genetics|November 1, 2011
Pathogenic aberrations revealed exclusively by single nucleotide polymorphism (SNP) genotyping data in 5000 samples tested by molecular karyotypingD L Bruno, S M White, D Ganesamoorthy, et al.
Pageof 43