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Nature Genetics|February 1, 1996
Nf1 deficiency causes Ras-mediated granulocyte/macrophage colony stimulating factor hypersensitivity and chronic myeloid leukaemiaD A Largaespada, C I Brannan, N A Jenkins, et al.Nature Genetics|February 1, 1996
Loss of NF1 results in activation of the Ras signaling pathway and leads to aberrant growth in haematopoietic cellsG Bollag, D W Clapp, S Shih, et al.Nature Genetics|February 1, 1996
Peg3 imprinted gene on proximal chromosome 7 encodes for a zinc finger proteinY Kuroiwa, T Kaneko-Ishino, F Kagitani, et al.Nature Genetics|February 1, 1996
The methyl-CpG binding protein MeCP2 is essential for embryonic development in the mouseP Tate, W Skarnes, A BirdNature Genetics|June 1, 1996
Identification of sex-specific quantitative trait loci controlling alcohol preference in C57BL/ 6 miceJ A Melo, J Shendure, K Pociask, et al.Nature Genetics|June 1, 1996
A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2C L Hanis, E Boerwinkle, R Chakraborty, et al.Nature Genetics|June 1, 1996
Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2D B Simon, F E Karet, J M Hamdan, et al.Nature Genetics|June 1, 1996
A functionally defective allele of TAP1 results in loss of MHC class I antigen presentation in a human lung cancerH L Chen, D Gabrilovich, R Tampé, et al.Nature Genetics|June 1, 1996
Low incidence of BRCA2 mutations in breast carcinoma and other cancersD H Teng, R Bogden, J Mitchell, et al.Pageof 745