K. Devon

Initial sequencing and analysis of the human genome.

J. V. Moran, V. J. Pollara, D. Haussler, 2001, Nature.

Erratum: Initial sequencing and analysis of the human genome: International Human Genome Sequencing Consortium (Nature (2001) 409 (860-921))

Ronald W. Davis, J. V. Moran, V. J. Pollara, 2001 .

An azoospermic man with a de novo point mutation in the Y-chromosomal gene USP9Y

B. Birren, D. Page, K. Devon, 1999, Nature Genetics.

The 1.4-Mb CMT1A duplication/HNPP deletion genomic region reveals unique genome architectural features and provides insights into the recent evolution of new genes.

B. Birren, E. Lander, J. Lupski, 2001, Genome research.

Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): high-resolution physical and transcript map of the candidate region in chromosome region 13q11.

B. Birren, T. Hudson, J. Rioux, 1999, 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.

Mouse molecular cytogenetic resource: 157 BACs link the chromosomal and genetic maps.

B. Birren, X. Chen, J. Korenberg, 1999, Genome research.