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Human Mutation|February 5, 2000
Molecular analysis of northwestern Mexican patients with cystic fibrosis: screening of 10 known mutations. Mutations in brief no. 185. OnlineS E Flores-Martínez, M Dean, R K Saiki, et al.Human Mutation|February 5, 2000
The minisatellite expansion mutation in EPM1: resolution of an initial discrepancy. Mutatations in brief no. 186. OnlineK Virtaneva, L Paulin, R Krahe, et al.Human Mutation|February 5, 2000
Laminin 5 genes and Herlitz junctional epidermolysis bullosa: novel mutations and polymorphisms in the LAMB3 and LAMC2 genes. Mutations in brief no. 190. OnlineA Kon, L Pulkkinen, M Hara, et al.Human Mutation|February 5, 2000
T426I a new mutation in the thyroid hormone receptor beta gene in a sporadic patient with resistance to thyroid hormone and dysmorphism. Mutations in brief no. 192. OnlineC Menzaghi, R Di Paola, A Corrias, et al.Human Mutation|February 12, 2000
Mutations of the human P gene associated with Type II oculocutaneous albinism (OCA2). Mutations in brief no. 205. OnlineW S Oetting, J M Gardner, J P Fryer, et al.Human Mutation|February 12, 2000
Twelve novel RB1 gene mutations in patients with hereditary retinoblastoma. Mutations in brief no. 206. OnlineS Yilmaz, B Horsthemke, D R LohmannHuman Mutation|January 29, 2000
Sequence variants of DLC1 in colorectal and ovarian tumoursP J Wilson, E McGlinn, A Marsh, et al.Human Mutation|January 29, 2000
Glucocerebrosidase gene mutations in patients with type 2 Gaucher diseaseD L Stone, N Tayebi, E Orvisky, et al.Human Mutation|July 17, 1999
Mutations of the VHL gene in sporadic renal cell carcinoma: definition of a risk factor for VHL patients to develop an RCCC Gallou, D Joly, A Méjean, et al.Human Mutation|July 17, 1999
Genomic structure and identification of 11 novel mutations of the PEX6 (peroxisome assembly factor-2) gene in patients with peroxisome biogenesis disordersZ Zhang, Y Suzuki, N Shimozawa, et al.Pageof 583