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Z Stark

Showing results (1-10 of 7) with videos related to

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Dyslexia (Chichester, England)|December 11, 2024
Validation and Reliability of the Dyslexia Adult Checklist in Screening for DyslexiaZ Stark, K Elalouf, V Soldano, et al.
The Journal of Hand Surgery|March 1, 1990
Electromyographic analysis of brachioradialis to flexor pollicis longus tendon transfer in quadriplegiaR L Waters, L Z Stark, I Gubernick, et al.
Journal of Neuroimmunology|March 10, 2001
Restricted IgG1 subclass of anti-Yo antibodies in paraneoplastic cerebellar degenerationE Amyes, J Curnow, Z Stark, et al.
Clinical Genetics|July 30, 2011
Two novel germline KRAS mutations: expanding the molecular and clinical phenotypeZ Stark, G Gillessen-Kaesbach, M M Ryan, et al.
Journal of Medical Genetics|November 1, 2011
Pathogenic aberrations revealed exclusively by single nucleotide polymorphism (SNP) genotyping data in 5000 samples tested by molecular karyotypingD L Bruno, S M White, D Ganesamoorthy, et al.
Molecular Syndromology|December 6, 2011
Sixteen New Cases Contributing to the Characterization of Patients with Distal 22q11.2 MicroduplicationsJ Wincent, D L Bruno, B W M van Bon, et al.
Human Mutation|November 7, 2009
Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndromeV Laugel, C Dalloz, M Durand, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Dyslexia (Chichester, England)|December 11, 2024
Validation and Reliability of the Dyslexia Adult Checklist in Screening for DyslexiaZ Stark, K Elalouf, V Soldano, et al.
The Journal of Hand Surgery|March 1, 1990
Electromyographic analysis of brachioradialis to flexor pollicis longus tendon transfer in quadriplegiaR L Waters, L Z Stark, I Gubernick, et al.
Journal of Neuroimmunology|March 10, 2001
Restricted IgG1 subclass of anti-Yo antibodies in paraneoplastic cerebellar degenerationE Amyes, J Curnow, Z Stark, et al.
Clinical Genetics|July 30, 2011
Two novel germline KRAS mutations: expanding the molecular and clinical phenotypeZ Stark, G Gillessen-Kaesbach, M M Ryan, et al.
Journal of Medical Genetics|November 1, 2011
Pathogenic aberrations revealed exclusively by single nucleotide polymorphism (SNP) genotyping data in 5000 samples tested by molecular karyotypingD L Bruno, S M White, D Ganesamoorthy, et al.
Molecular Syndromology|December 6, 2011
Sixteen New Cases Contributing to the Characterization of Patients with Distal 22q11.2 MicroduplicationsJ Wincent, D L Bruno, B W M van Bon, et al.
Human Mutation|November 7, 2009
Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndromeV Laugel, C Dalloz, M Durand, et al.
Pageof 1