Human molecular genetics - JoVE Visualize

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Human Molecular Genetics|November 18, 1998

Mosaicism in sporadic neurofibromatosis 2 patientsL Kluwe, V F Mautner

Human Molecular Genetics|November 18, 1998

Hereditary lymphedema: evidence for linkage and genetic heterogeneityR E Ferrell, K L Levinson, J H Esman, et al.

Human Molecular Genetics|November 18, 1998

NF2 gene in neurofibromatosis type 2 patientsJ Zucman-Rossi, P Legoix, H Der Sarkissian, et al.

Human Molecular Genetics|November 18, 1998

Calcitonin receptor polymorphism is associated with a decreased fracture risk in post-menopausal womenJ Taboulet, M Frenkian, J L Frendo, et al.

Human Molecular Genetics|December 1, 1996

Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxiasG Stevanin, Y Trottier, G Cancel, et al.

Human Molecular Genetics|December 1, 1996

Identification of two mutations in a compound heterozygous child with dihydrolipoamide dehydrogenase deficiencyY S Hong, D S Kerr, W J Craigen, et al.

Human Molecular Genetics|December 1, 1996

An extended region of biallelic gene expression and rodent-human synteny downstream of the imprinted H19 gene on chromosome 11p15.5L Yuan, N Qian, B Tycko

Human Molecular Genetics|December 1, 1996

Frameshift mutation in the survival motor neuron gene in a severe case of SMA type IC Brahe, O Clermont, S Zappata, et al.

Human Molecular Genetics|December 1, 1996

Molecular and biochemical analysis of protective protein/cathepsin A mutations: correlation with clinical severity in galactosialidosisX Y Zhou, A van der Spoel, R Rottier, et al.

Human Molecular Genetics|December 1, 1996

Evidence for subtelomeric exchange of 3.3 kb tandemly repeated units between chromosomes 4q35 and 10q26: implications for genetic counselling and etiology of FSHD1J C van Deutekom, E Bakker, R J Lemmers, et al.

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Showing results (441-450 of 11,953) with videos related to

Sort By:

Pageof 1,196

Human Molecular Genetics|November 18, 1998

Mosaicism in sporadic neurofibromatosis 2 patientsL Kluwe, V F Mautner

Human Molecular Genetics|November 18, 1998

Hereditary lymphedema: evidence for linkage and genetic heterogeneityR E Ferrell, K L Levinson, J H Esman, et al.

Human Molecular Genetics|November 18, 1998

NF2 gene in neurofibromatosis type 2 patientsJ Zucman-Rossi, P Legoix, H Der Sarkissian, et al.

Human Molecular Genetics|November 18, 1998

Calcitonin receptor polymorphism is associated with a decreased fracture risk in post-menopausal womenJ Taboulet, M Frenkian, J L Frendo, et al.

Human Molecular Genetics|December 1, 1996

Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxiasG Stevanin, Y Trottier, G Cancel, et al.

Human Molecular Genetics|December 1, 1996

Identification of two mutations in a compound heterozygous child with dihydrolipoamide dehydrogenase deficiencyY S Hong, D S Kerr, W J Craigen, et al.

Human Molecular Genetics|December 1, 1996

An extended region of biallelic gene expression and rodent-human synteny downstream of the imprinted H19 gene on chromosome 11p15.5L Yuan, N Qian, B Tycko

Human Molecular Genetics|December 1, 1996

Frameshift mutation in the survival motor neuron gene in a severe case of SMA type IC Brahe, O Clermont, S Zappata, et al.

Human Molecular Genetics|December 1, 1996

Molecular and biochemical analysis of protective protein/cathepsin A mutations: correlation with clinical severity in galactosialidosisX Y Zhou, A van der Spoel, R Rottier, et al.

Human Molecular Genetics|December 1, 1996

Evidence for subtelomeric exchange of 3.3 kb tandemly repeated units between chromosomes 4q35 and 10q26: implications for genetic counselling and etiology of FSHD1J C van Deutekom, E Bakker, R J Lemmers, et al.

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