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Nadav Agam

Showing results (11-20 of 15) with videos related to

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Clinical Genetics|July 21, 2022
PSMC1 variant causes a novel neurological syndromeSarit Aharoni, Regina Proskorovski-Ohayon, Ramesh Kumar Krishnan, et al.
NPJ Genomic Medicine|October 10, 2025
A ciliopathy combining Joubert syndrome and Oro-Facial-Digital syndrome caused by bi-allelic 5'-UTR loss-of-function CEP83 variantMatan M Jean, Anan Yunis, Tzofit Elbaz-Biton, et al.
Human Genetics|April 12, 2024
VARista: a free web platform for streamlined whole-genome variant analysis across T2T, hg38, and hg19Noam Hadar, Vadim Dolgin, Katya Oustinov, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 10, 2025
Early-Onset Movement Disorder Syndrome Caused by Biallelic Variants in PDE1B Encoding Phosphodiesterase 1BTomer Poleg, Noam Hadar, Eyal Kristal, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|August 15, 2025
Intronic and Coding Genetic Variants in Autosomal Recessive Polycystic Kidney Disease Among Israeli Bedouins of Arabian Peninsula AncestryNadav Agam, Ohad Wormser, Ari Biller, et al.
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Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Clinical Genetics|July 21, 2022
PSMC1 variant causes a novel neurological syndromeSarit Aharoni, Regina Proskorovski-Ohayon, Ramesh Kumar Krishnan, et al.
NPJ Genomic Medicine|October 10, 2025
A ciliopathy combining Joubert syndrome and Oro-Facial-Digital syndrome caused by bi-allelic 5'-UTR loss-of-function CEP83 variantMatan M Jean, Anan Yunis, Tzofit Elbaz-Biton, et al.
Human Genetics|April 12, 2024
VARista: a free web platform for streamlined whole-genome variant analysis across T2T, hg38, and hg19Noam Hadar, Vadim Dolgin, Katya Oustinov, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 10, 2025
Early-Onset Movement Disorder Syndrome Caused by Biallelic Variants in PDE1B Encoding Phosphodiesterase 1BTomer Poleg, Noam Hadar, Eyal Kristal, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|August 15, 2025
Intronic and Coding Genetic Variants in Autosomal Recessive Polycystic Kidney Disease Among Israeli Bedouins of Arabian Peninsula AncestryNadav Agam, Ohad Wormser, Ari Biller, et al.
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