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Nature Genetics|March 1, 1997
Cloning, expression and chromosomal mapping of human lysosomal sialidase and characterization of mutations in sialidosisA V Pshezhetsky, C Richard, L Michaud, et al.Nature Genetics|April 1, 1997
Genome cross-referencing and XREFdb: implications for the identification and analysis of genes mutated in human diseaseD E Bassett, M S Boguski, F Spencer, et al.Nature Genetics|April 1, 1997
A high observed substitution rate in the human mitochondrial DNA control regionT J Parsons, D S Muniec, K Sullivan, et al.Nature Genetics|April 1, 1997
Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctataN Braverman, G Steel, C Obie, et al.Nature Genetics|April 1, 1997
Rhizomelic chondrodysplasia punctata is a peroxisomal protein targeting disease caused by a non-functional PTS2 receptorA M Motley, E H Hettema, E M Hogenhout, et al.Nature Genetics|April 1, 1997
Isolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disordersC C Chang, W H Lee, H Moser, et al.Nature Genetics|May 1, 1997
Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndromeE Rao, B Weiss, M Fukami, et al.Nature Genetics|May 1, 1997
Chemotherapy induces transient sex chromosomal and autosomal aneuploidy in human spermW A Robbins, M L Meistrich, D Moore, et al.Nature Genetics|May 1, 1997
The parentage of a classic wine grape, Cabernet SauvignonJ E Bowers, C P MeredithNature Genetics|May 1, 1997
Emerin deletion reveals a common X-chromosome inversion mediated by inverted repeatsK Small, J Iber, S T WarrenPageof 742