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Medrxiv : the Preprint Server for Health Sciences
|
October 7, 2024
Heterozygous loss-of-function variants in SPTAN1 cause a novel early childhood onset distal myopathy with chronic neurogenic features
Jonathan De Winter, Liedewei Van de Vondel, Biljana Ermanoska, et al.
Acta Neuropathologica
|
January 15, 2021
Making sense of missense variants in TTN-related congenital myopathies
Martin Rees, Roksana Nikoopour, Atsushi Fukuzawa, et al.
Human Mutation
|
June 18, 2019
Deleterious de novo variants of X-linked ZC4H2 in females cause a variable phenotype with neurogenic arthrogryposis multiplex congenita
Suzanna G M Frints, Friederike Hennig, Roberto Colombo, et al.
Human Mutation
|
April 3, 2014
Mutation update and genotype-phenotype correlations of novel and previously described mutations in TPM2 and TPM3 causing congenital myopathies
Minttu Marttila, Vilma-Lotta Lehtokari, Steven Marston, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 19, 2019
A clinical scoring system for congenital contractural arachnodactyly
Ilse Meerschaut, Shana De Coninck, Wouter Steyaert, et al.
Neurology. Genetics
|
August 17, 2023
Clinical Classification of Variants in the Valosin-Containing Protein Gene Associated With Multisystem Proteinopathy
Marianela Schiava, Chiseko Ikenaga, Ana Topf, et al.
Human Mutation
|
April 23, 2013
ANO5 gene analysis in a large cohort of patients with anoctaminopathy: confirmation of male prevalence and high occurrence of the common exon 5 gene mutation
Anna Sarkozy, Debbie Hicks, Judith Hudson, et al.
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Search research articles
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Showing results (51-60 of 57) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 57 results.
Medrxiv : the Preprint Server for Health Sciences
|
October 7, 2024
Heterozygous loss-of-function variants in SPTAN1 cause a novel early childhood onset distal myopathy with chronic neurogenic features
Jonathan De Winter, Liedewei Van de Vondel, Biljana Ermanoska, et al.
Acta Neuropathologica
|
January 15, 2021
Making sense of missense variants in TTN-related congenital myopathies
Martin Rees, Roksana Nikoopour, Atsushi Fukuzawa, et al.
Human Mutation
|
June 18, 2019
Deleterious de novo variants of X-linked ZC4H2 in females cause a variable phenotype with neurogenic arthrogryposis multiplex congenita
Suzanna G M Frints, Friederike Hennig, Roberto Colombo, et al.
Human Mutation
|
April 3, 2014
Mutation update and genotype-phenotype correlations of novel and previously described mutations in TPM2 and TPM3 causing congenital myopathies
Minttu Marttila, Vilma-Lotta Lehtokari, Steven Marston, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 19, 2019
A clinical scoring system for congenital contractural arachnodactyly
Ilse Meerschaut, Shana De Coninck, Wouter Steyaert, et al.
Neurology. Genetics
|
August 17, 2023
Clinical Classification of Variants in the Valosin-Containing Protein Gene Associated With Multisystem Proteinopathy
Marianela Schiava, Chiseko Ikenaga, Ana Topf, et al.
Human Mutation
|
April 23, 2013
ANO5 gene analysis in a large cohort of patients with anoctaminopathy: confirmation of male prevalence and high occurrence of the common exon 5 gene mutation
Anna Sarkozy, Debbie Hicks, Judith Hudson, et al.
Page
of 6