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Spectrum of<i>MKS1</i>and<i>MKS3</i>mutations in Meckel syndrome: a genotype-phenotype correlation af Rana Khaddour, Ursula M. Smith, Lekbir Baala, Jéléna Martinovic, Davina Clavering, Rizwana Shaffiq, Catherine Ozilou, Andrew R. Cullinane, Mira Kyttälä, Stavit A. Shalev, Sophie Audollent, Camille d’Humières, Noman Kadhom, Chantal Esculpavit, Géraldine Viot, Claire Boone, Christine Oien, Férechté Encha‐Razavi, P A Batman, Christopher Bennett, C. Geoffrey Woods, J. Roume, Stanislas Lyonnet, Emmanuelle Génin, Martine Le Merrer, Arnold Münnich, Marie‐Claire Gubler, P. Cox, Fiona MacDonald, Michel Vekemans, Colin A. Johnson, Tania Attié‐Bitach
Udgivet 2007Artigo
Søgeredskaber:
Relaterede emner
Biology
Atrophy
Biopsy
Coeliac disease
Compound heterozygosity
Disease
Dysplasia
Enteropathy
Epithelium
Gene
Genetic heterogeneity
Genetics
Genotype
Histology
Hyperplasia
Immune system
Immunology
Immunopathology
Internal medicine
Intestinal mucosa
Intraepithelial lymphocyte
Lamina propria
Medicine
Mutation
Pathology
Phenotype
Polydactyly
Villous atrophy
Virus