Resultados de procura - Mark Houseman
- Mostrando 1 - 4 Resultados de 4
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1
Connexin Mutations in Skin Disease and Hearing Loss por David P. Kelsell, Wei‐Li Di, Mark Houseman
Publicado 2001Revisão -
2
Baseline serum MMP-3 levels in patients with Rheumatoid Arthritis are still independently predictive of radiographic progression in a longitudinal observational cohort at 8 years f... por Mark Houseman, Catherine Potter, Nicolette Marshall, Rachel Lakey, Tim Cawston, I D Griffiths, Steven Young‐Min, John D. Isaacs
Publicado 2012Artigo -
3
Genetic analysis of the connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing loss por Mark Houseman, Lucy Ellis, Alistair T. Pagnamenta, Wei‐Li Di, Sarah Rickard, Amelia H. Osborn, H Dahl, Graham R. Taylor, M. Bitner-Glindzicz, William Reardon, R F Mueller, David P. Kelsell
Publicado 2001Artigo -
4
Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene por Françoise Denoyelle, Dominique Weil, Marion A. Maw, S.A. Wilcox, Nicholas Lench, D. R. Allen-Powell, Amelia H. Osborn, H Dahl, Anna Middleton, Mark Houseman, Catherine Dodé, Sandrine Marlin, Amel Boulila‐Elgaied, M’hamed Grati, Hammadi Ayadi, S. Benarab, Pierre Bitoun, Geneviève Lina‐Granade, Jacqueline Godet, Mirna Mustapha, Jacques Loiselet, Elie El‐Zir, Anne Aubois, A Joannard, Jacqueline Levilliers, E.N. Garabédian, R F Mueller, R. J McKinlay Gardner, Christine Petit
Publicado 1997Artigo
Ferramentas de procura:
Materias Relacionadas
Biology
Gene
Genetics
Allele
Connexin
Gap junction
Intracellular
Locus (genetics)
Medicine
Mutation
Allele frequency
Anatomy
Audiology
Baseline (sea)
Cell biology
Coding region
Cohort
Cohort study
Compound heterozygosity
Connexin 32
Cytoplasm
Environmental health
Epidermis (zoology)
Genetic linkage
Genotype
Geology
Haplotype
Hearing loss
Internal medicine
Microsatellite