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Sharon Zeligson

Showing results (31-40 of 37) with videos related to

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Neurology|February 12, 2017
Vesicular acetylcholine transporter defect underlies devastating congenital myasthenia syndromeAdi Aran, Reeval Segel, Kota Kaneshige, et al.
The New England Journal of Medicine|September 13, 2018
Essential Role of BRCA2 in Ovarian Development and FunctionAriella Weinberg-Shukron, Mariana Rachmiel, Paul Renbaum, et al.
Neurology|May 11, 2016
Loss of function of PCDH12 underlies recessive microcephaly mimicking intrauterine infectionAdi Aran, Nuphar Rosenfeld, Ranit Jaron, et al.
Journal of Medical Genetics|May 17, 2018
Mitochondrial <i>PITRM1</i> peptidase loss-of-function in childhood cerebellar atrophyYeshaya Langer, Adi Aran, Suleyman Gulsuner, et al.
Journal of Medical Genetics|July 29, 2021
Diagnostic yield of chromosomal microarray and trio whole exome sequencing in cryptogenic cerebral palsyMichal Yechieli, Suleyman Gulsuner, Hilla Ben-Pazi, et al.
Blood|December 8, 2009
Down syndrome acute lymphoblastic leukemia, a highly heterogeneous disease in which aberrant expression of CRLF2 is associated with mutated JAK2: a report from the International BFM Study GroupLibi Hertzberg, Elena Vendramini, Ithamar Ganmore, et al.
The New England Journal of Medicine|February 21, 2014
Mutant adenosine deaminase 2 in a polyarteritis nodosa vasculopathyPaulina Navon Elkan, Sarah B Pierce, Reeval Segel, et al.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Neurology|February 12, 2017
Vesicular acetylcholine transporter defect underlies devastating congenital myasthenia syndromeAdi Aran, Reeval Segel, Kota Kaneshige, et al.
The New England Journal of Medicine|September 13, 2018
Essential Role of BRCA2 in Ovarian Development and FunctionAriella Weinberg-Shukron, Mariana Rachmiel, Paul Renbaum, et al.
Neurology|May 11, 2016
Loss of function of PCDH12 underlies recessive microcephaly mimicking intrauterine infectionAdi Aran, Nuphar Rosenfeld, Ranit Jaron, et al.
Journal of Medical Genetics|May 17, 2018
Mitochondrial <i>PITRM1</i> peptidase loss-of-function in childhood cerebellar atrophyYeshaya Langer, Adi Aran, Suleyman Gulsuner, et al.
Journal of Medical Genetics|July 29, 2021
Diagnostic yield of chromosomal microarray and trio whole exome sequencing in cryptogenic cerebral palsyMichal Yechieli, Suleyman Gulsuner, Hilla Ben-Pazi, et al.
Blood|December 8, 2009
Down syndrome acute lymphoblastic leukemia, a highly heterogeneous disease in which aberrant expression of CRLF2 is associated with mutated JAK2: a report from the International BFM Study GroupLibi Hertzberg, Elena Vendramini, Ithamar Ganmore, et al.
The New England Journal of Medicine|February 21, 2014
Mutant adenosine deaminase 2 in a polyarteritis nodosa vasculopathyPaulina Navon Elkan, Sarah B Pierce, Reeval Segel, et al.
Pageof 4