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Nature Genetics|May 1, 1996
Exclusive paternal origin of new mutations in Apert syndromeD M Moloney, S F Slaney, M Oldridge, et al.Nature Genetics|May 1, 1996
High frequency de novo alterations in the long-range genomic structure of the mouse pseudoautosomal regionD Kipling, E C Salido, L J Shapiro, et al.Nature Genetics|May 1, 1996
Cloning and expression of the mouse pseudoautosomal steroid sulphatase gene (Sts)E C Salido, X M Li, P H Yen, et al.Nature Genetics|May 1, 1996
Epigenetic modifications during oocyte growth correlates with extended parthenogenetic development in the mouseT Kono, Y Obata, T Yoshimzu, et al.Nature Genetics|May 1, 1996
Severe autosomal dominant hypertension and brachydactyly in a unique Turkish kindred maps to human chromosome 12H Schuster, T E Wienker, S Bähring, et al.Nature Genetics|July 1, 1996
The molecular basis of hypodactyly (Hd): a deletion in Hoxa 13 leads to arrest of digital arch formationD P Mortlock, L C Post, J W InnisNature Genetics|July 1, 1996
Accelerated telomere shortening in ataxia telangiectasiaJ A Metcalfe, J Parkhill, L Campbell, et al.Nature Genetics|July 1, 1996
Missense mutation in the gene encoding the alpha subunit of rod transducin in the Nougaret form of congenital stationary night blindnessT P Dryja, L B Hahn, T Reboul, et al.Nature Genetics|July 1, 1996
Epithelial detachment due to absence of hemidesmosomes in integrin beta 4 null miceR van der Neut, P Krimpenfort, J Calafat, et al.Nature Genetics|May 1, 1993
Genomic mismatch scanning: a new approach to genetic linkage mappingS F Nelson, J H McCusker, M A Sander, et al.Pageof 745