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Nature Genetics|August 2, 2001
Mutations in the region encoding the von Willebrand factor A domain of matrilin-3 are associated with multiple epiphyseal dysplasiaK L Chapman, G R Mortier, K Chapman, et al.Nature Genetics|July 1, 1992
Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expressionJ Wagstaff, J H Knoll, K A Glatt, et al.Nature Genetics|October 1, 1992
Periodic paralysis in quarter horses: a sodium channel mutation disseminated by selective breedingJ A Rudolph, S J Spier, G Byrns, et al.Nature Genetics|November 1, 1992
Large scale cDNA sequencing for analysis of quantitative and qualitative aspects of gene expressionK Okubo, N Hori, R Matoba, et al.Nature Genetics|November 1, 1992
Expression of Xist in mouse germ cells correlates with X-chromosome inactivationJ R McCarrey, D D DilworthNature Genetics|November 1, 1992
Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in FinlandJ Hästbacka, A de la Chapelle, I Kaitila, et al.Nature Genetics|June 11, 1992
The peripheral myelin gene PMP-22/GAS-3 is duplicated in Charcot-Marie-Tooth disease type 1AL J Valentijn, P A Bolhuis, I Zorn, et al.Nature Genetics|September 1, 1992
Molecular evolution of the human interleukin-8 receptor gene clusterS K Ahuja, T Ozçelik, A Milatovitch, et al.Nature Genetics|September 1, 1992
A frameshift mutation in the gamma E-crystallin gene of the Elo mouseM Cartier, M L Breitman, L C TsuiNature Genetics|September 1, 1992
Distinct and overlapping functions of allelic forms of human mannose binding proteinM Super, S D Gillies, S Foley, et al.Pageof 744