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Nature Genetics|September 1, 1995
Interaction between undulated and Patch leads to an extreme form of spina bifida in double-mutant miceU Helwig, K Imai, W Schmahl, et al.Nature Genetics|September 1, 1995
MSH2 deficient mice are viable and susceptible to lymphoid tumoursA H Reitmair, R Schmits, A Ewel, et al.Nature Genetics|September 1, 1995
Hypertension caused by a truncated epithelial sodium channel gamma subunit: genetic heterogeneity of Liddle syndromeJ H Hansson, C Nelson-Williams, H Suzuki, et al.Nature Genetics|October 1, 1995
Quantitative locus analysis of airway hyperresponsiveness in A/J and C57BL/6J miceG T De Sanctis, M Merchant, D R Beier, et al.Nature Genetics|October 1, 1995
Mice lacking ornithine-delta-aminotransferase have paradoxical neonatal hypoornithinaemia and retinal degenerationT Wang, A M Lawler, G Steel, et al.Nature Genetics|October 1, 1995
Genomic imprinting of p57KIP2, a cyclin-dependent kinase inhibitor, in mouseI Hatada, T MukaiNature Genetics|October 1, 1995
Genetic association of the very low density lipoprotein (VLDL) receptor gene with sporadic Alzheimer's diseaseK Okuizumi, O Onodera, Y Namba, et al.Nature Genetics|October 1, 1995
The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21-q24P Paavola, R Salonen, J Weissenbach, et al.Nature Genetics|November 1, 1994
A second locus for Marfan syndrome maps to chromosome 3p24.2-p25G Collod, M C Babron, G Jondeau, et al.Nature Genetics|May 1, 1995
Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated formY Trottier, D Devys, G Imbert, et al.Pageof 745