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Genetic determinants of diastolic and pulse pressure map to different loci in Lyon hypertensive rats
National licenceNature Publishing Group | 1993| -
A modular approach for integrative analysis of large-scale gene-expression and drug-response data
Online Contents | 2008|Contributors: Beckmann, Jacques S. -
A gene for familial juvenile nephronophthisis (recessive medullary cystic kidney disease) maps to chromosome 2p
National licenceNature Publishing Group | 1993| -
Molecular and cellular basis of calpainopathy (limb girdle muscular dystrophy type 2A)
Online Contents | 2007|Contributors: Beckmann, Jacques S. -
β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12
National licenceNature Publishing Group | 1995| -
Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome
National licenceNature Publishing Group | 1999| -
Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy
National licenceElsevier | 1994| -
Dysferlin is a Plasma Membrane Protein and is Expressed Early in Human Development
Oxford University Press | 1999| -
Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IκBα/NF-κB pathway in limb-girdle muscular dystrophy type 2A
National licenceNature Publishing Group | 1999| -
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B
National licenceNature Publishing Group | 1998| -
The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy
National licenceNature Publishing Group | 2001| -
Transcription Factor CTF1 Acts as a Chromatin Domain Boundary That Shields Human Telomeric Genes from Silencing
Online Contents | 2009|Contributors: Beckmann, Jacques S.
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