Gerd Scherer

Point mutations in the tyrosine aminotransferase gene in tyrosinemia type II.

M. Di Rocco, G. Scherer, M. Odiévre, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Comparative genomics of the SOX9 region in human and Fugu rubripes: conservation of short regulatory sequence elements within large intergenic regions.

C. Ferraz, J. Demaille, G. Scherer, 2001, Genomics.

Campomelic dysplasia translocation breakpoints are scattered over 1 Mb proximal to SOX9: evidence for an extended control region.

B. Birren, E. Lander, K. Dewar, 1999, American journal of human genetics.

The SOX8 gene is located within 700 kb of the tip of chromosome 16p and is deleted in a patient with ATR-16 syndrome.

F. Kooy, G. Scherer, F. Poulat, 2000, Genomics.

A 45,X male with a Yp/18 translocation

J. Weissenbach, W. Schempp, M. Fraccaro, 1986, Human Genetics.

Identification of a locus which shows no genetic recombination with the autosomal dominant polycystic kidney disease gene on chromosome 16.

J. Lamb, Y. Nakamura, G. Germino, 1990, American journal of human genetics.

The SOX10/Sox10 gene from human and mouse: sequence, expression, and transactivation by the encoded HMG domain transcription factor

B. Roe, R. Balling, R. Kist, 1998, Human Genetics.