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A Rafiq

Showing results (91-100 of 98) with videos related to

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Clinical Genetics|August 1, 2014
Phosphoserine phosphatase (PSPH) gene mutation in an intellectual disability family from PakistanJ B Vincent, T Jamil, M A Rafiq, et al.
Human Molecular Genetics|March 15, 2014
Disruption of the methyltransferase-like 23 gene METTL23 causes mild autosomal recessive intellectual disabilityMarie Bernkopf, Gerald Webersinke, Chanakan Tongsook, et al.
Nature Genetics|November 23, 2006
Genome assembly comparison identifies structural variants in the human genomeRazi Khaja, Junjun Zhang, Jeffrey R MacDonald, et al.
European Heart Journal|September 22, 2018
An autoantibody identifies arrhythmogenic right ventricular cardiomyopathy and participates in its pathogenesisDiptendu Chatterjee, Meena Fatah, Deniz Akdis, et al.
PLOS Digital Health|January 9, 2025
A data management system for precision medicineJohn J L Jacobs, Inés Beekers, Inge Verkouter, et al.
Molecular Psychiatry|April 12, 2017
Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous familiesR Harripaul, N Vasli, A Mikhailov, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 8, 2022
PPA2-associated sudden cardiac death: extending the clinical and allelic spectrum in 20 new familiesAnne Guimier, Melanie T Achleitner, Anne Moreau de Bellaing, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 17, 2021
PPA2-associated sudden cardiac death: extending the clinical and allelic spectrum in 20 new familiesAnne Guimier, Melanie T Achleitner, Anne Moreau de Bellaing, et al.
Pageof 10

Showing results (91-100 of 98) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 98 results.
Clinical Genetics|August 1, 2014
Phosphoserine phosphatase (PSPH) gene mutation in an intellectual disability family from PakistanJ B Vincent, T Jamil, M A Rafiq, et al.
Human Molecular Genetics|March 15, 2014
Disruption of the methyltransferase-like 23 gene METTL23 causes mild autosomal recessive intellectual disabilityMarie Bernkopf, Gerald Webersinke, Chanakan Tongsook, et al.
Nature Genetics|November 23, 2006
Genome assembly comparison identifies structural variants in the human genomeRazi Khaja, Junjun Zhang, Jeffrey R MacDonald, et al.
European Heart Journal|September 22, 2018
An autoantibody identifies arrhythmogenic right ventricular cardiomyopathy and participates in its pathogenesisDiptendu Chatterjee, Meena Fatah, Deniz Akdis, et al.
PLOS Digital Health|January 9, 2025
A data management system for precision medicineJohn J L Jacobs, Inés Beekers, Inge Verkouter, et al.
Molecular Psychiatry|April 12, 2017
Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous familiesR Harripaul, N Vasli, A Mikhailov, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 8, 2022
PPA2-associated sudden cardiac death: extending the clinical and allelic spectrum in 20 new familiesAnne Guimier, Melanie T Achleitner, Anne Moreau de Bellaing, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 17, 2021
PPA2-associated sudden cardiac death: extending the clinical and allelic spectrum in 20 new familiesAnne Guimier, Melanie T Achleitner, Anne Moreau de Bellaing, et al.
Pageof 10