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Genomics|February 18, 1998
Sequence characterization of a newly identified human alpha-tubulin gene (TUBA2)C Dodé, D Weil, J Levilliers, et al.Human Molecular Genetics|June 1, 1994
A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 geneP Guilford, H Ayadi, S Blanchard, et al.Gut|March 9, 2005
Chromoendoscopic surveillance in hereditary diffuse gastric cancer: an alternative to prophylactic gastrectomy?D Shaw, V Blair, A Framp, et al.Genomics|September 1, 1995
A YAC contig and an EST map in the pericentromeric region of chromosome 13 surrounding the loci for neurosensory nonsyndromic deafness (DFNB1 and DFNA3) and limb-girdle muscular dystrophy type 2C (LGMD2C)P Guilford, C Dodé, F Crozet, et al.Nature|March 2, 1995
Defective myosin VIIA gene responsible for Usher syndrome type 1BD Weil, S Blanchard, J Kaplan, et al.Nature|April 16, 1998
E-cadherin germline mutations in familial gastric cancerP Guilford, J Hopkins, J Harraway, et al.Revista Espanola De Enfermedades Digestivas|March 25, 2006
Single nucleotide polymorphisms (SNPs) at CDH1 promoter region in familial gastric cancerA Ramos-de la Medina, H More, H Medina-Franco, et al.Carcinogenesis|June 5, 1999
Familial gastric cancer: clinicopathological characteristics, RER phenotype and germline p53 and E-cadherin mutationsK Shinmura, T Kohno, M Takahashi, et al.Gynecologic Oncology|December 20, 2011
Adrenomedullin interacts with VEGF in endometrial cancer and has varied modulation in tumours of different gradesJ J Evans, K Chitcholtan, J M Dann, et al.Human Mutation|January 16, 2007
Identification of seven novel germline mutations in the human E-cadherin (CDH1) geneH More, B Humar, W Weber, et al.Pageof 3