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Arie Koifman

Showing results (21-30 of 24) with videos related to

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European Journal of Human Genetics : EJHG|May 11, 2017
Progressive hereditary spastic paraplegia caused by a homozygous KY mutationYuval Yogev, Yonatan Perez, Iris Noyman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 26, 2025
A founder variant in TBCB is associated with global developmental delay, autism spectrum and spastic paraparesisSharon Bratman Morag, Chen Itzkovich, Alina Kurolap, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 4, 2020
Teaching clinicians practical genomic medicine: 7 years' experience in a tertiary care centerRachel Michaelson-Cohen, Liat Salzer-Sheelo, Rivka Sukenik-Halevy, et al.
JAMA Network Open|February 22, 2024
National Rapid Genome Sequencing in Neonatal Intensive CareDaphna Marom, Adi Mory, Sivan Reytan-Miron, et al.
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Showing results (21-30 of 24) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 24 results.
European Journal of Human Genetics : EJHG|May 11, 2017
Progressive hereditary spastic paraplegia caused by a homozygous KY mutationYuval Yogev, Yonatan Perez, Iris Noyman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 26, 2025
A founder variant in TBCB is associated with global developmental delay, autism spectrum and spastic paraparesisSharon Bratman Morag, Chen Itzkovich, Alina Kurolap, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 4, 2020
Teaching clinicians practical genomic medicine: 7 years' experience in a tertiary care centerRachel Michaelson-Cohen, Liat Salzer-Sheelo, Rivka Sukenik-Halevy, et al.
JAMA Network Open|February 22, 2024
National Rapid Genome Sequencing in Neonatal Intensive CareDaphna Marom, Adi Mory, Sivan Reytan-Miron, et al.
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