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Maria Elena Hernandez Gonzalez

Showing results (1-10 of 6) with videos related to

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Scientific Reports|October 25, 2024
Defining the transcriptome of PIK3CA-altered cells in a human capillary malformation using single cell long-read sequencingMichelle A Wedemeyer, Tianli Ding, Elizabeth A R Garfinkle, et al.
Human Mutation|December 3, 2021
Long-read whole genome sequencing reveals HOXD13 alterations in synpolydactylyMarilena Melas, Esko A Kautto, Samuel J Franklin, et al.
BMC Genomics|May 24, 2011
Analysis of expressed sequence tags generated from full-length enriched cDNA libraries of melonChristian Clepet, Tarek Joobeur, Yi Zheng, et al.
Cold Spring Harbor Molecular Case Studies|February 12, 2022
Expanding the clinical phenotype of <i>FGFR1</i> internal tandem duplicationEsko A Kautto, Kathleen M Schieffer, Sean McGrath, et al.
Medrxiv : the Preprint Server for Health Sciences|May 7, 2026
Optical genome mapping identifies clinically relevant somatic structural variation in epilepsy-affected brain tissueAnthony R Miller, James J Anderson, Maria Elena Hernandez Gonzalez, et al.
Acta Neuropathologica Communications|April 8, 2021
Molecular classification of a complex structural rearrangement of the RB1 locus in an infant with sporadic, isolated, intracranial, sellar region retinoblastomaKathleen M Schieffer, Alexander Z Feldman, Esko A Kautto, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Scientific Reports|October 25, 2024
Defining the transcriptome of PIK3CA-altered cells in a human capillary malformation using single cell long-read sequencingMichelle A Wedemeyer, Tianli Ding, Elizabeth A R Garfinkle, et al.
Human Mutation|December 3, 2021
Long-read whole genome sequencing reveals HOXD13 alterations in synpolydactylyMarilena Melas, Esko A Kautto, Samuel J Franklin, et al.
BMC Genomics|May 24, 2011
Analysis of expressed sequence tags generated from full-length enriched cDNA libraries of melonChristian Clepet, Tarek Joobeur, Yi Zheng, et al.
Cold Spring Harbor Molecular Case Studies|February 12, 2022
Expanding the clinical phenotype of <i>FGFR1</i> internal tandem duplicationEsko A Kautto, Kathleen M Schieffer, Sean McGrath, et al.
Medrxiv : the Preprint Server for Health Sciences|May 7, 2026
Optical genome mapping identifies clinically relevant somatic structural variation in epilepsy-affected brain tissueAnthony R Miller, James J Anderson, Maria Elena Hernandez Gonzalez, et al.
Acta Neuropathologica Communications|April 8, 2021
Molecular classification of a complex structural rearrangement of the RB1 locus in an infant with sporadic, isolated, intracranial, sellar region retinoblastomaKathleen M Schieffer, Alexander Z Feldman, Esko A Kautto, et al.
Pageof 1