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Nature Genetics|September 1, 1994
Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control regionJ S Sutcliffe, M Nakao, S Christian, et al.Nature Genetics|September 1, 1994
Identification of mutations in the alpha 3(IV) and alpha 4(IV) collagen genes in autosomal recessive Alport syndromeT Mochizuki, H H Lemmink, M Mariyama, et al.Nature Genetics|June 1, 1994
The origin of the major cystic fibrosis mutation (delta F508) in European populationsN Morral, J Bertranpetit, X Estivill, et al.Nature Genetics|June 1, 1994
Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer diseaseE H Corder, A M Saunders, N J Risch, et al.Nature Genetics|July 1, 1994
Tumour predisposition in mice heterozygous for a targeted mutation in Nf1T Jacks, T S Shih, E M Schmitt, et al.Nature Genetics|July 1, 1994
Highly homologous loci on the X and Y chromosomes are hot-spots for ectopic recombinations leading to XX malenessD Weil, I Wang, A Dietrich, et al.Nature Genetics|July 1, 1994
High resolution localization of recombination hot spots using sperm typingR Hubert, M MacDonald, J Gusella, et al.Nature Genetics|July 1, 1994
Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35A Hentati, K Bejaoui, M A Pericak-Vance, et al.Nature Genetics|July 1, 1994
Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21-cenK Zerres, G Mücher, L Bachner, et al.Nature Genetics|July 1, 1994
Epigenetic lesions at the H19 locus in Wilms' tumour patientsT Moulton, T Crenshaw, Y Hao, et al.Pageof 744