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Karin Weiss

Showing results (11-20 of 59) with videos related to

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Journal of Child Neurology|July 21, 2007
Congenital myopathies in Israeli familiesKarin Weiss, Yehuda Shapira, Benjamin Glick, et al.
European Journal of Medical Genetics|February 7, 2024
Rapid exome sequencing for children with severe acute encephalopathy - A case seriesClair Habib, Tamar Paperna, Rinat Zaid, et al.
Rambam Maimonides Medical Journal|August 9, 2018
Rare Disease Diagnostics: A Single-center Experience and Lessons LearntKarin Weiss, Alina Kurolap, Tamar Paperna, et al.
Pediatric Blood & Cancer|November 20, 2025
IKAROS Associated Immunodeficiency and Thrombotic Thrombocytopenic PurpuraIlia Spivak, Daniella Magen, Karin Weiss, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 31, 2014
Ethnic effect on FMR1 carrier rate and AGG repeat interruptions among Ashkenazi womenKarin Weiss, Avi Orr-Urtreger, Idit Kaplan Ber, et al.
European Journal of Medical Genetics|May 23, 2021
Concomitant congenital CMV infection and inherited liver diseasesRana Swed-Tobia, Imad Kassis, Karin Weiss, et al.
Familial Cancer|May 17, 2021
A recurrent pathogenic BRCA2 exon 5-11 duplication in the Christian Arab population in IsraelGili Reznick Levi, Gal Larom, Vered Ofen Glassner, et al.
European Child & Adolescent Psychiatry|December 23, 2017
Refugees in Europe: national overviews from key countries with a special focus on child and adolescent mental healthMatthew Hodes, Melisa Mendoza Vasquez, Dimitris Anagnostopoulos, et al.
Frontiers in Neurology|August 15, 2020
<i>SETD5</i> Gene Haploinsufficiency in Three Patients With Suspected KBG SyndromeMilena Crippa, Ilaria Bestetti, Silvia Maitz, et al.
American Journal of Human Genetics|April 23, 2019
A CCR4-NOT Transcription Complex, Subunit 1, CNOT1, Variant Associated with HoloprosencephalyPaul Kruszka, Seth I Berger, Karin Weiss, et al.
Pageof 6

Showing results (11-20 of 59) with videos related to

Sort By:
Pageof 6
Journal of Child Neurology|July 21, 2007
Congenital myopathies in Israeli familiesKarin Weiss, Yehuda Shapira, Benjamin Glick, et al.
European Journal of Medical Genetics|February 7, 2024
Rapid exome sequencing for children with severe acute encephalopathy - A case seriesClair Habib, Tamar Paperna, Rinat Zaid, et al.
Rambam Maimonides Medical Journal|August 9, 2018
Rare Disease Diagnostics: A Single-center Experience and Lessons LearntKarin Weiss, Alina Kurolap, Tamar Paperna, et al.
Pediatric Blood & Cancer|November 20, 2025
IKAROS Associated Immunodeficiency and Thrombotic Thrombocytopenic PurpuraIlia Spivak, Daniella Magen, Karin Weiss, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 31, 2014
Ethnic effect on FMR1 carrier rate and AGG repeat interruptions among Ashkenazi womenKarin Weiss, Avi Orr-Urtreger, Idit Kaplan Ber, et al.
European Journal of Medical Genetics|May 23, 2021
Concomitant congenital CMV infection and inherited liver diseasesRana Swed-Tobia, Imad Kassis, Karin Weiss, et al.
Familial Cancer|May 17, 2021
A recurrent pathogenic BRCA2 exon 5-11 duplication in the Christian Arab population in IsraelGili Reznick Levi, Gal Larom, Vered Ofen Glassner, et al.
European Child & Adolescent Psychiatry|December 23, 2017
Refugees in Europe: national overviews from key countries with a special focus on child and adolescent mental healthMatthew Hodes, Melisa Mendoza Vasquez, Dimitris Anagnostopoulos, et al.
Frontiers in Neurology|August 15, 2020
<i>SETD5</i> Gene Haploinsufficiency in Three Patients With Suspected KBG SyndromeMilena Crippa, Ilaria Bestetti, Silvia Maitz, et al.
American Journal of Human Genetics|April 23, 2019
A CCR4-NOT Transcription Complex, Subunit 1, CNOT1, Variant Associated with HoloprosencephalyPaul Kruszka, Seth I Berger, Karin Weiss, et al.
Pageof 6