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Clinical genetics

Showing results (671-680 of 7,173) with videos related to

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Clinical Genetics|April 19, 2011
Mutations in WDR62, encoding a centrosomal and nuclear protein, in Indian primary microcephaly families with cortical malformationsV Bhat, S C Girimaji, G Mohan, et al.
Clinical Genetics|June 24, 2011
Using Alzheimer's disease as a model for genetic risk disclosure: implications for personal genomicsJ S Roberts, K D Christensen, R C Green
Clinical Genetics|June 24, 2011
Genotype-phenotype correlation in colorectal polyposisK F Newton, E K L Mallinson, J Bowen, et al.
Clinical Genetics|December 16, 2010
Characterization of two Ashkenazi Jewish founder mutations in MSH6 gene causing Lynch syndromeL Raskin, F Schwenter, M Freytsis, et al.
Clinical Genetics|December 24, 2010
Congenital myasthenic syndrome associated with epidermolysis bullosa caused by homozygous mutations in PLEC1 and CHRNER A Maselli, J Arredondo, O Cagney, et al.
Clinical Genetics|January 5, 2011
Breast cancer after bilateral risk-reducing mastectomyA-B Skytte, D Crüger, M Gerster, et al.
Clinical Genetics|March 3, 2011
BAG3-related myofibrillar myopathy in a Chinese familyH C Lee, S W Cherk, S K Chan, et al.
Clinical Genetics|February 26, 2011
Novel glucokinase mutations in patients with monogenic diabetes - clinical outline of GCK-MD and potential for founder effect in Slavic populationM Borowiec, K Antosik, W Fendler, et al.
Clinical Genetics|January 26, 2011
Childhood brain tumours due to germline bi-allelic mismatch repair gene mutationsP C Johannesma, H M van der Klift, N C T van Grieken, et al.
Clinical Genetics|January 25, 2011
Clinical, biochemical and molecular characterization of cystinuria in a cohort of 12 patientsM Barbosa, A Lopes, C Mota, et al.
Pageof 718

Showing results (671-680 of 7,173) with videos related to

Sort By:
Pageof 718
Clinical Genetics|April 19, 2011
Mutations in WDR62, encoding a centrosomal and nuclear protein, in Indian primary microcephaly families with cortical malformationsV Bhat, S C Girimaji, G Mohan, et al.
Clinical Genetics|June 24, 2011
Using Alzheimer's disease as a model for genetic risk disclosure: implications for personal genomicsJ S Roberts, K D Christensen, R C Green
Clinical Genetics|June 24, 2011
Genotype-phenotype correlation in colorectal polyposisK F Newton, E K L Mallinson, J Bowen, et al.
Clinical Genetics|December 16, 2010
Characterization of two Ashkenazi Jewish founder mutations in MSH6 gene causing Lynch syndromeL Raskin, F Schwenter, M Freytsis, et al.
Clinical Genetics|December 24, 2010
Congenital myasthenic syndrome associated with epidermolysis bullosa caused by homozygous mutations in PLEC1 and CHRNER A Maselli, J Arredondo, O Cagney, et al.
Clinical Genetics|January 5, 2011
Breast cancer after bilateral risk-reducing mastectomyA-B Skytte, D Crüger, M Gerster, et al.
Clinical Genetics|March 3, 2011
BAG3-related myofibrillar myopathy in a Chinese familyH C Lee, S W Cherk, S K Chan, et al.
Clinical Genetics|February 26, 2011
Novel glucokinase mutations in patients with monogenic diabetes - clinical outline of GCK-MD and potential for founder effect in Slavic populationM Borowiec, K Antosik, W Fendler, et al.
Clinical Genetics|January 26, 2011
Childhood brain tumours due to germline bi-allelic mismatch repair gene mutationsP C Johannesma, H M van der Klift, N C T van Grieken, et al.
Clinical Genetics|January 25, 2011
Clinical, biochemical and molecular characterization of cystinuria in a cohort of 12 patientsM Barbosa, A Lopes, C Mota, et al.
Pageof 718