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Christopher Walsh

Showing results (51-60 of 59) with videos related to

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Epilepsia|January 19, 2006
Mutation in filamin A causes periventricular heterotopia, developmental regression, and West syndrome in malesMarcelo R Masruha, Luis O S F Caboclo, Henrique Carrete, et al.
Nature|April 8, 2025
Author Correction: Recapitulation of premature ageing with iPSCs from Hutchinson-Gilford progeria syndromeGuang-Hui Liu, Basam Z Barkho, Sergio Ruiz, et al.
Nature|February 25, 2011
Recapitulation of premature ageing with iPSCs from Hutchinson-Gilford progeria syndromeGuang-Hui Liu, Basam Z Barkho, Sergio Ruiz, et al.
Blood Advances|October 3, 2024
Real-world impact of emicizumab and immunosuppression on acquired hemophilia A: a multicenter US cohortJacqueline N Poston, Cassandra Bryan, Annette von Drygalski, et al.
Cardiovascular Research|July 31, 2012
Developmental basis for filamin-A-associated myxomatous mitral valve diseaseKimberly Sauls, Annemarieke de Vlaming, Brett S Harris, et al.
American Journal of Human Genetics|May 14, 2019
Bi-allelic Variants in DYNC1I2 Cause Syndromic Microcephaly with Intellectual Disability, Cerebral Malformations, and Dysmorphic Facial FeaturesMuhammad Ansar, Farid Ullah, Sohail A Paracha, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
A comprehensive view of somatic mosaicism by single-cell DNA analysisLovelace J Luquette, Tim H H Coorens, Abhiram Natu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 15, 2018
Genomic and phenotypic delineation of congenital microcephalyRanad Shaheen, Sateesh Maddirevula, Nour Ewida, et al.
European Journal of Human Genetics : EJHG|June 21, 2023
BRAT1-related disorders: phenotypic spectrum and phenotype-genotype correlations from 97 patientsCamille Engel, Stéphanie Valence, Geoffroy Delplancq, et al.
Pageof 6

Showing results (51-60 of 59) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 59 results.
Epilepsia|January 19, 2006
Mutation in filamin A causes periventricular heterotopia, developmental regression, and West syndrome in malesMarcelo R Masruha, Luis O S F Caboclo, Henrique Carrete, et al.
Nature|April 8, 2025
Author Correction: Recapitulation of premature ageing with iPSCs from Hutchinson-Gilford progeria syndromeGuang-Hui Liu, Basam Z Barkho, Sergio Ruiz, et al.
Nature|February 25, 2011
Recapitulation of premature ageing with iPSCs from Hutchinson-Gilford progeria syndromeGuang-Hui Liu, Basam Z Barkho, Sergio Ruiz, et al.
Blood Advances|October 3, 2024
Real-world impact of emicizumab and immunosuppression on acquired hemophilia A: a multicenter US cohortJacqueline N Poston, Cassandra Bryan, Annette von Drygalski, et al.
Cardiovascular Research|July 31, 2012
Developmental basis for filamin-A-associated myxomatous mitral valve diseaseKimberly Sauls, Annemarieke de Vlaming, Brett S Harris, et al.
American Journal of Human Genetics|May 14, 2019
Bi-allelic Variants in DYNC1I2 Cause Syndromic Microcephaly with Intellectual Disability, Cerebral Malformations, and Dysmorphic Facial FeaturesMuhammad Ansar, Farid Ullah, Sohail A Paracha, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
A comprehensive view of somatic mosaicism by single-cell DNA analysisLovelace J Luquette, Tim H H Coorens, Abhiram Natu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 15, 2018
Genomic and phenotypic delineation of congenital microcephalyRanad Shaheen, Sateesh Maddirevula, Nour Ewida, et al.
European Journal of Human Genetics : EJHG|June 21, 2023
BRAT1-related disorders: phenotypic spectrum and phenotype-genotype correlations from 97 patientsCamille Engel, Stéphanie Valence, Geoffroy Delplancq, et al.
Pageof 6