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Showing results (71-80 of 75) with videos related to

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Progres En Urologie : Journal De L'Association Francaise D'Urologie Et De La Societe Francaise D'Urologie|November 6, 2020
Prospective multicentre observational study assessing the tolerance and perception of patients using the Liquick Base catheter with an Ergothan tipX Gamé, L Gania, B Perrouin-Verbe, et al.
Human Molecular Genetics|March 21, 1998
Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansionJ Del-Favero, L Krols, A Michalik, et al.
Neurology|September 30, 2010
Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutationsL Deprez, S Weckhuysen, P Holmgren, et al.
Neurology|September 30, 2010
Mutations in SACS cause atypical and late-onset forms of ARSACSJ Baets, T Deconinck, K Smets, et al.
Clinical Genetics|July 12, 2008
Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11N Hilgert, F Alasti, N Dieltjens, et al.
Pageof 8

Showing results (71-80 of 75) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 75 results.
Progres En Urologie : Journal De L'Association Francaise D'Urologie Et De La Societe Francaise D'Urologie|November 6, 2020
Prospective multicentre observational study assessing the tolerance and perception of patients using the Liquick Base catheter with an Ergothan tipX Gamé, L Gania, B Perrouin-Verbe, et al.
Human Molecular Genetics|March 21, 1998
Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansionJ Del-Favero, L Krols, A Michalik, et al.
Neurology|September 30, 2010
Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutationsL Deprez, S Weckhuysen, P Holmgren, et al.
Neurology|September 30, 2010
Mutations in SACS cause atypical and late-onset forms of ARSACSJ Baets, T Deconinck, K Smets, et al.
Clinical Genetics|July 12, 2008
Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11N Hilgert, F Alasti, N Dieltjens, et al.
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