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Showing results (531-540 of 536) with videos related to

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Genes & Development|July 15, 1996
Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organizationW H McLean, L Pulkkinen, F J Smith, et al.
Nature Genetics|August 1, 1996
Plectin deficiency results in muscular dystrophy with epidermolysis bullosaF J Smith, R A Eady, I M Leigh, et al.
The Journal of Investigative Dermatology|August 21, 2001
The spectrum of pathogenic mutations in SPINK5 in 19 families with Netherton syndrome: implications for mutation detection and first case of prenatal diagnosisE Sprecher, S Chavanas, J J DiGiovanna, et al.
The British Journal of Dermatology|February 5, 2020
Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragilityC Has, J W Bauer, C Bodemer, et al.
Journal of Molecular Medicine (Berlin, Germany)|April 12, 2000
A 500-kb region on chromosome 16p13.1 contains the pseudoxanthoma elasticum locus: high-resolution mapping and genomic structureL Cai, B Struk, M D Adams, et al.
The British Journal of Dermatology|June 7, 2019
Genotype-phenotype correlation in a large English cohort of patients with autosomal recessive ichthyosisJ K Simpson, M Martinez-Queipo, A Onoufriadis, et al.
Pageof 54

Showing results (531-540 of 536) with videos related to

Sort By:
Pageof 54
You have reached the last page of results.This site can display upto 536 results.
Genes & Development|July 15, 1996
Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organizationW H McLean, L Pulkkinen, F J Smith, et al.
Nature Genetics|August 1, 1996
Plectin deficiency results in muscular dystrophy with epidermolysis bullosaF J Smith, R A Eady, I M Leigh, et al.
The Journal of Investigative Dermatology|August 21, 2001
The spectrum of pathogenic mutations in SPINK5 in 19 families with Netherton syndrome: implications for mutation detection and first case of prenatal diagnosisE Sprecher, S Chavanas, J J DiGiovanna, et al.
The British Journal of Dermatology|February 5, 2020
Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragilityC Has, J W Bauer, C Bodemer, et al.
Journal of Molecular Medicine (Berlin, Germany)|April 12, 2000
A 500-kb region on chromosome 16p13.1 contains the pseudoxanthoma elasticum locus: high-resolution mapping and genomic structureL Cai, B Struk, M D Adams, et al.
The British Journal of Dermatology|June 7, 2019
Genotype-phenotype correlation in a large English cohort of patients with autosomal recessive ichthyosisJ K Simpson, M Martinez-Queipo, A Onoufriadis, et al.
Pageof 54