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Clinical genetics

Showing results (71-80 of 9,192) with videos related to

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Clinical Genetics|November 26, 2013
Clinical spectrum and molecular basis of recessive congenital methemoglobinemia in IndiaP P Warang, P S Kedar, C Shanmukaiah, et al.
Clinical Genetics|November 22, 2012
Knowledge of the Genetic Information Nondiscrimination act among individuals affected by Huntington diseaseE R Dorsey, K C Darwin, P E Nichols, et al.
Clinical Genetics|November 21, 2012
Perspectives of clinical genetics professionals toward genome sequencing and incidental findings: a survey studyA A Lemke, D Bick, D Dimmock, et al.
Clinical Genetics|November 22, 2012
Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesisA Mostowska, B Biedziak, M Zadurska, et al.
Clinical Genetics|September 5, 2015
Mutation spectrum of the MTM1 gene in XLMTM patients: 10 years of experience in prenatal and postnatal diagnosisG Longo, S Russo, G Novelli, et al.
Clinical Genetics|July 1, 1989
X-linked myotubular myopathy: clinical and pathological findings in a familyA Oldfors, M Kyllerman, J Wahlström, et al.
Clinical Genetics|January 29, 2016
High frequency of OTOF mutations in Chinese infants with congenital auditory neuropathy spectrum disorderQ-J Zhang, B Han, L Lan, et al.
Clinical Genetics|February 3, 2016
Clinical, biochemical and molecular characterization of prosaposin deficiencyM Motta, M Tatti, F Furlan, et al.
Clinical Genetics|January 16, 2016
A non-sense MCM9 mutation in a familial case of primary ovarian insufficiencyF Fauchereau, S Shalev, E Chervinsky, et al.
Clinical Genetics|January 13, 2016
Diagnostic odyssey in severe neurodevelopmental disorders: toward clinical whole-exome sequencing as a first-line diagnostic testJ Thevenon, Y Duffourd, A Masurel-Paulet, et al.
Pageof 920

Showing results (71-80 of 9,192) with videos related to

Sort By:
Pageof 920
Clinical Genetics|November 26, 2013
Clinical spectrum and molecular basis of recessive congenital methemoglobinemia in IndiaP P Warang, P S Kedar, C Shanmukaiah, et al.
Clinical Genetics|November 22, 2012
Knowledge of the Genetic Information Nondiscrimination act among individuals affected by Huntington diseaseE R Dorsey, K C Darwin, P E Nichols, et al.
Clinical Genetics|November 21, 2012
Perspectives of clinical genetics professionals toward genome sequencing and incidental findings: a survey studyA A Lemke, D Bick, D Dimmock, et al.
Clinical Genetics|November 22, 2012
Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesisA Mostowska, B Biedziak, M Zadurska, et al.
Clinical Genetics|September 5, 2015
Mutation spectrum of the MTM1 gene in XLMTM patients: 10 years of experience in prenatal and postnatal diagnosisG Longo, S Russo, G Novelli, et al.
Clinical Genetics|July 1, 1989
X-linked myotubular myopathy: clinical and pathological findings in a familyA Oldfors, M Kyllerman, J Wahlström, et al.
Clinical Genetics|January 29, 2016
High frequency of OTOF mutations in Chinese infants with congenital auditory neuropathy spectrum disorderQ-J Zhang, B Han, L Lan, et al.
Clinical Genetics|February 3, 2016
Clinical, biochemical and molecular characterization of prosaposin deficiencyM Motta, M Tatti, F Furlan, et al.
Clinical Genetics|January 16, 2016
A non-sense MCM9 mutation in a familial case of primary ovarian insufficiencyF Fauchereau, S Shalev, E Chervinsky, et al.
Clinical Genetics|January 13, 2016
Diagnostic odyssey in severe neurodevelopmental disorders: toward clinical whole-exome sequencing as a first-line diagnostic testJ Thevenon, Y Duffourd, A Masurel-Paulet, et al.
Pageof 920