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Nature Genetics|April 1, 1995
A paternal-specific methylation imprint marks the alleles of the mouse H19 geneK D Tremblay, J R Saam, R S Ingram, et al.Nature Genetics|May 1, 1993
New mdx mutation disrupts expression of muscle and nonmuscle isoforms of dystrophinG A Cox, S F Phelps, V M Chapman, et al.Nature Genetics|March 1, 1994
Altered cleavage and secretion of a recombinant beta-APP bearing the Swedish familial Alzheimer's disease mutationK M Felsenstein, L W Hunihan, S B RobertsNature Genetics|March 1, 1994
X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locusP Saugier-Veber, A Munnich, D Bonneau, et al.Nature Genetics|March 1, 1994
A frame shift mutation in the PMP22 gene in hereditary neuropathy with liability to pressure palsiesG A Nicholson, L J Valentijn, A K Cherryson, et al.Nature Genetics|March 1, 1994
Genomic instability in repeated sequences is an early somatic event in colorectal tumorigenesis that persists after transformationD Shibata, M A Peinado, Y Ionov, et al.Nature Genetics|March 1, 1994
Mosaic and polymorphic imprinting of the WT1 gene in humansY Jinno, K Yun, K Nishiwaki, et al.Nature Genetics|March 1, 1994
The gene for achondroplasia maps to the telomeric region of chromosome 4pM Velinov, S A Slaugenhaupt, I Stoilov, et al.Nature Genetics|August 1, 1994
PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defectsT Glaser, L Jepeal, J G Edwards, et al.Nature Genetics|August 1, 1994
The murine Xe169 gene escapes X-inactivation like its human homologueJ Wu, E C Salido, P H Yen, et al.Pageof 743