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J Senderek

Showing results (21-30 of 25) with videos related to

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Clinical Genetics|April 9, 2015
Diagnostic algorithms in Charcot-Marie-Tooth neuropathies: experiences from a German genetic laboratory on the basis of 1206 index patientsS Rudnik-Schöneborn, D Tölle, J Senderek, et al.
Clinical Genetics|June 28, 2017
Extension of the phenotype of biallelic loss-of-function mutations in SLC25A46 to the severe form of pontocerebellar hypoplasia type IM C Braunisch, H Gallwitz, A Abicht, et al.
Clinical Genetics|July 21, 2018
Novel SBF2 mutations and clinical spectrum of Charcot-Marie-Tooth neuropathy type 4B2P Laššuthová, K Vill, S Erdem-Ozdamar, et al.
Neurology|August 23, 2006
Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutationsH Azzedine, N Ravisé, C Verny, et al.
Neuromuscular Disorders : NMD|October 22, 2017
Molecular characterization of congenital myasthenic syndromes in SpainD Natera-de Benito, A Töpf, J J Vilchez, et al.
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Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
Clinical Genetics|April 9, 2015
Diagnostic algorithms in Charcot-Marie-Tooth neuropathies: experiences from a German genetic laboratory on the basis of 1206 index patientsS Rudnik-Schöneborn, D Tölle, J Senderek, et al.
Clinical Genetics|June 28, 2017
Extension of the phenotype of biallelic loss-of-function mutations in SLC25A46 to the severe form of pontocerebellar hypoplasia type IM C Braunisch, H Gallwitz, A Abicht, et al.
Clinical Genetics|July 21, 2018
Novel SBF2 mutations and clinical spectrum of Charcot-Marie-Tooth neuropathy type 4B2P Laššuthová, K Vill, S Erdem-Ozdamar, et al.
Neurology|August 23, 2006
Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutationsH Azzedine, N Ravisé, C Verny, et al.
Neuromuscular Disorders : NMD|October 22, 2017
Molecular characterization of congenital myasthenic syndromes in SpainD Natera-de Benito, A Töpf, J J Vilchez, et al.
Pageof 3