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Ina Amarillo

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Medical Oncology (Northwood, London, England)|November 28, 2014
BRCA2-associated therapy-related acute myeloid leukemiaArmin Rashidi, Ina Amarillo, Stephen I Fisher
Clinics in Laboratory Medicine|November 29, 2011
Solid tumor cytogenetics: current perspectivesGouri Nanjangud, Ina Amarillo, P Nagesh Rao
American Journal of Medical Genetics. Part A|December 28, 2020
Pathogenic paternally inherited NLGN4X deletion in a female with autism spectrum disorder: Clinical, cytogenetic, and molecular characterizationNathan Kopp, Ina Amarillo, Julian Martinez-Agosto, et al.
European Journal of Medical Genetics|August 19, 2019
Intragenic CNTN4 copy number variants associated with a spectrum of neurobehavioral phenotypesStephanie Q Zhang, Julie Fleischer, Hussam Al-Kateb, et al.
Journal of Clinical Research in Pediatric Endocrinology|May 10, 2018
Inherited Deletion of 1q, Hyperparathyroidism and Signs of Y-chromosomal Influence in a Patient with Turner SyndromeAlejandro F. Siller, Alex Shimony, Marwan Shinawi, et al.
Molecular Cytogenetics|February 2, 2013
Atypical rearrangement involving 3'-IGH@ and a breakpoint at least 400 Kb upstream of an intact MYC in a CLL patient with an apparently balanced t(8;14)(q24.1;q32) and negative MYC expressionIna Amarillo, Peter H Bui, Sibel Kantarci, et al.
Journal of Medical Genetics|June 11, 2020
Rare and <i>de novo</i> duplications containing <i>SHOX</i> in clubfootBrooke Sadler, Gabe Haller, Lilian Antunes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 16, 2022
Words matter: The language of difference in human geneticsMildred K Cho, Maria Laura Duque Lasio, Ina Amarillo, et al.
The Journal of Molecular Diagnostics : JMD|May 17, 2025
Path to Health Equity and Improved Outcomes through Inclusive Sex and Gender Data Collection in Genomic TestingMarco L Leung, Ina Amarillo, Danielle Jordan, et al.
Cancer Genetics|December 6, 2023
Clinical whole-genome sequencing and FISH identify two different fusion partners for NUP98 in a patient with acute myeloid leukemia: A case reportBahareh A Mojarad, Zachary D Crees, Molly C Schroeder, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Medical Oncology (Northwood, London, England)|November 28, 2014
BRCA2-associated therapy-related acute myeloid leukemiaArmin Rashidi, Ina Amarillo, Stephen I Fisher
Clinics in Laboratory Medicine|November 29, 2011
Solid tumor cytogenetics: current perspectivesGouri Nanjangud, Ina Amarillo, P Nagesh Rao
American Journal of Medical Genetics. Part A|December 28, 2020
Pathogenic paternally inherited NLGN4X deletion in a female with autism spectrum disorder: Clinical, cytogenetic, and molecular characterizationNathan Kopp, Ina Amarillo, Julian Martinez-Agosto, et al.
European Journal of Medical Genetics|August 19, 2019
Intragenic CNTN4 copy number variants associated with a spectrum of neurobehavioral phenotypesStephanie Q Zhang, Julie Fleischer, Hussam Al-Kateb, et al.
Journal of Clinical Research in Pediatric Endocrinology|May 10, 2018
Inherited Deletion of 1q, Hyperparathyroidism and Signs of Y-chromosomal Influence in a Patient with Turner SyndromeAlejandro F. Siller, Alex Shimony, Marwan Shinawi, et al.
Molecular Cytogenetics|February 2, 2013
Atypical rearrangement involving 3'-IGH@ and a breakpoint at least 400 Kb upstream of an intact MYC in a CLL patient with an apparently balanced t(8;14)(q24.1;q32) and negative MYC expressionIna Amarillo, Peter H Bui, Sibel Kantarci, et al.
Journal of Medical Genetics|June 11, 2020
Rare and <i>de novo</i> duplications containing <i>SHOX</i> in clubfootBrooke Sadler, Gabe Haller, Lilian Antunes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 16, 2022
Words matter: The language of difference in human geneticsMildred K Cho, Maria Laura Duque Lasio, Ina Amarillo, et al.
The Journal of Molecular Diagnostics : JMD|May 17, 2025
Path to Health Equity and Improved Outcomes through Inclusive Sex and Gender Data Collection in Genomic TestingMarco L Leung, Ina Amarillo, Danielle Jordan, et al.
Cancer Genetics|December 6, 2023
Clinical whole-genome sequencing and FISH identify two different fusion partners for NUP98 in a patient with acute myeloid leukemia: A case reportBahareh A Mojarad, Zachary D Crees, Molly C Schroeder, et al.
Pageof 2