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Nature Genetics|April 1, 1996
Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3J S Colvin, B A Bohne, G W Harding, et al.Nature Genetics|April 1, 1996
A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order AmishE I Ginns, J Ott, J A Egeland, et al.Nature Genetics|April 1, 1996
Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome)P Edery, T Attié, J Amiel, et al.Nature Genetics|April 1, 1996
A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)R M Hofstra, J Osinga, G Tan-Sindhunata, et al.Nature Genetics|April 1, 1996
Inactivation of Fac in mice produces inducible chromosomal instability and reduced fertility reminiscent of Fanconi anaemiaM Chen, D J Tomkins, W Auerbach, et al.Nature Genetics|September 1, 1993
Hemizygosity at the elastin locus in a developmental disorder, Williams syndromeA K Ewart, C A Morris, D Atkinson, et al.Nature Genetics|July 1, 1995
Cloning of the galactokinase cDNA and identification of mutations in two families with cataractsD Stambolian, Y Ai, D Sidjanin, et al.Nature Genetics|July 1, 1995
Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindredsN A Gruis, P A van der Velden, L A Sandkuijl, et al.Nature Genetics|July 1, 1995
Assignment of dominant inherited nocturnal enuresis (ENUR1) to chromosome 13qH Eiberg, I Berendt, J MohrNature Genetics|August 1, 1995
Gene-based sequence-tagged-sites (STSs) as the basis for a human gene mapR Berry, T J Stevens, N A Walter, et al.Pageof 745