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Karin Writzl

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American Journal of Medical Genetics. Part A|May 21, 2013
6p21.3 microdeletion involving the SYNGAP1 gene in a patient with intellectual disability, seizures, and severe speech impairmentKarin Writzl, Alida C Knegt
Fertility and Sterility|November 9, 2005
Copy number of DAZ genes in infertile menKarin Writzl, Branko Zorn, Borut Peterlin
American Journal of Medical Genetics. Part A|September 19, 2009
Interstitial deletion 2p11.2-p12: further delineationKarin Writzl, Luca Lovrecić, Borut Peterlin
Clinical Dysmorphology|February 24, 2017
Co-occurrence of rhabdomyosarcoma and Mowat-Wilson syndrome: is there a connection?Mihael Rogac, Lidija Kitanovski, Karin Writzl
Collegium Antropologicum|December 2, 2004
Copy number of DAZ genes in Slovenian and Bosnian general populationKarin Writzl, Amela Sehić, Rifet Terzić, et al.
Journal of Community Genetics|January 16, 2021
Improving diagnostics of rare genetic diseases with NGS approachesMateja Vinkšel, Karin Writzl, Aleš Maver, et al.
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association|December 21, 2021
Preceding Head Trauma in Four Cases of Sporadic Cerebral Amyloid Angiopathy - Case Report SeriesJanja Pretnar Oblak, Ana Jurečič, Karin Writzl, et al.
Plos One|November 4, 2024
Genetic background of high myopia in childrenUrh Šenk, Bernard Čižman, Karin Writzl, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 6, 2015
Early-onset epileptic encephalopathy with hearing loss in two siblings with TBC1D24 recessive mutationsBarbara Gnidovec Stražišar, David Neubauer, Darja Paro Panjan, et al.
Frontiers in Genetics|August 3, 2023
Case Report: Non-ossifying fibromas with pathologic fractures in a patient with <i>NONO</i>-associated X-linked syndromic intellectual developmental disorderKarin Writzl, Blaž Mavčič, Aleš Maver, et al.
Pageof 5

Showing results (1-10 of 43) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics. Part A|May 21, 2013
6p21.3 microdeletion involving the SYNGAP1 gene in a patient with intellectual disability, seizures, and severe speech impairmentKarin Writzl, Alida C Knegt
Fertility and Sterility|November 9, 2005
Copy number of DAZ genes in infertile menKarin Writzl, Branko Zorn, Borut Peterlin
American Journal of Medical Genetics. Part A|September 19, 2009
Interstitial deletion 2p11.2-p12: further delineationKarin Writzl, Luca Lovrecić, Borut Peterlin
Clinical Dysmorphology|February 24, 2017
Co-occurrence of rhabdomyosarcoma and Mowat-Wilson syndrome: is there a connection?Mihael Rogac, Lidija Kitanovski, Karin Writzl
Collegium Antropologicum|December 2, 2004
Copy number of DAZ genes in Slovenian and Bosnian general populationKarin Writzl, Amela Sehić, Rifet Terzić, et al.
Journal of Community Genetics|January 16, 2021
Improving diagnostics of rare genetic diseases with NGS approachesMateja Vinkšel, Karin Writzl, Aleš Maver, et al.
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association|December 21, 2021
Preceding Head Trauma in Four Cases of Sporadic Cerebral Amyloid Angiopathy - Case Report SeriesJanja Pretnar Oblak, Ana Jurečič, Karin Writzl, et al.
Plos One|November 4, 2024
Genetic background of high myopia in childrenUrh Šenk, Bernard Čižman, Karin Writzl, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 6, 2015
Early-onset epileptic encephalopathy with hearing loss in two siblings with TBC1D24 recessive mutationsBarbara Gnidovec Stražišar, David Neubauer, Darja Paro Panjan, et al.
Frontiers in Genetics|August 3, 2023
Case Report: Non-ossifying fibromas with pathologic fractures in a patient with <i>NONO</i>-associated X-linked syndromic intellectual developmental disorderKarin Writzl, Blaž Mavčič, Aleš Maver, et al.
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