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Showing results (91-100 of 100) with videos related to

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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 3, 2017
Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavinG Heimer, E Eyal, X Zhu, et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine|November 18, 1998
The clinical value of squamous cell carcinoma antigen in cancer of the uterine cervixH W de Bruijn, J M Duk, A G van der Zee, et al.
Clinical Genetics|April 5, 2016
A role for TENM1 mutations in congenital general anosmiaA Alkelai, T Olender, R Haffner-Krausz, et al.
Clinical Genetics|July 4, 2015
SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosumG Heimer, D Marek-Yagel, E Eyal, et al.
American Journal of Human Genetics|March 1, 1996
Linkage disequilibrium mapping places the gene causing familial Mediterranean fever close to D16S246E N Levy, Y Shen, A Kupelian, et al.
International Journal of Cancer|April 6, 2001
MLH1 and MSH2 protein expression as a pre-screening marker in hereditary and non-hereditary endometrial hyperplasia and cancerM J Berends, H Hollema, Y Wu, et al.
Human Molecular Genetics|February 7, 2001
Functional analysis of mutations in SLC7A9, and genotype-phenotype correlation in non-Type I cystinuriaM A Font, L Feliubadaló, X Estivill, et al.
Genomics|May 15, 1997
Construction of a 1-Mb restriction-mapped cosmid contig containing the candidate region for the familial Mediterranean fever locus (MEFV) on chromosome 16p 13.3R Sood, T Blake, I Aksentijevich, et al.
Genomics|November 5, 1997
A high-resolution genetic map of the familial Mediterranean fever candidate region allows identification of haplotype-sharing among ethnic groupsJ E Balow, D A Shelton, A Orsborn, et al.
Nature Genetics|September 2, 1999
Non-type I cystinuria caused by mutations in SLC7A9, encoding a subunit (bo,+AT) of rBATL Feliubadaló, M Font, J Purroy, et al.
Pageof 10

Showing results (91-100 of 100) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 100 results.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 3, 2017
Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavinG Heimer, E Eyal, X Zhu, et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine|November 18, 1998
The clinical value of squamous cell carcinoma antigen in cancer of the uterine cervixH W de Bruijn, J M Duk, A G van der Zee, et al.
Clinical Genetics|April 5, 2016
A role for TENM1 mutations in congenital general anosmiaA Alkelai, T Olender, R Haffner-Krausz, et al.
Clinical Genetics|July 4, 2015
SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosumG Heimer, D Marek-Yagel, E Eyal, et al.
American Journal of Human Genetics|March 1, 1996
Linkage disequilibrium mapping places the gene causing familial Mediterranean fever close to D16S246E N Levy, Y Shen, A Kupelian, et al.
International Journal of Cancer|April 6, 2001
MLH1 and MSH2 protein expression as a pre-screening marker in hereditary and non-hereditary endometrial hyperplasia and cancerM J Berends, H Hollema, Y Wu, et al.
Human Molecular Genetics|February 7, 2001
Functional analysis of mutations in SLC7A9, and genotype-phenotype correlation in non-Type I cystinuriaM A Font, L Feliubadaló, X Estivill, et al.
Genomics|May 15, 1997
Construction of a 1-Mb restriction-mapped cosmid contig containing the candidate region for the familial Mediterranean fever locus (MEFV) on chromosome 16p 13.3R Sood, T Blake, I Aksentijevich, et al.
Genomics|November 5, 1997
A high-resolution genetic map of the familial Mediterranean fever candidate region allows identification of haplotype-sharing among ethnic groupsJ E Balow, D A Shelton, A Orsborn, et al.
Nature Genetics|September 2, 1999
Non-type I cystinuria caused by mutations in SLC7A9, encoding a subunit (bo,+AT) of rBATL Feliubadaló, M Font, J Purroy, et al.
Pageof 10