Glen A. Evans

Affiliations: 
Salk Institute for Biological Studies, La Jolla, CA, United States 
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"Glen Evans"
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Legius E, Wlodarska I, Selleri L, et al. (2008) De novo 46,XX, dir dup (11)(q13.3→q14.2) in a patient with mental retardation, congenital cardiopathy and thrombopenia Clinical Genetics. 49: 206-210
Takada T, Kumánovics A, Amadou C, et al. (2003) Species-specific class I gene expansions formed the telomeric 1 Mb of the mouse major histocompatibility complex Genome Research. 13: 589-600
Hermanson GG, Evans GA. (2001) Rescuing YAC-insert ends as E. coli plasmids. Current Protocols in Human Genetics. Unit 5.8
Lane RP, Cutforth T, Young J, et al. (2001) Genomic analysis of orthologous mouse and human olfactory receptor loci. Proceedings of the National Academy of Sciences of the United States of America. 98: 7390-5
Lander ES, Linton LM, Birren B, et al. (2001) Initial sequencing and analysis of the human genome. Nature. 409: 860-921
Lander ES, Linton LM, Birren B, et al. (2001) Erratum: Initial sequencing and analysis of the human genome: International Human Genome Sequencing Consortium (Nature (2001) 409 (860-921)) Nature. 412: 565-566
Stickens D, Brown D, Evans GA. (2000) EXT genes are differentially expressed in bone and cartilage during mouse embryogenesis. Developmental Dynamics. 218: 452-464
Pulido HA, Fakruddin MJ, Chatterjee A, et al. (2000) Identification of a 6-cM Minimal Deletion at 11q23.1–23.2 and Exclusion of PPP2R1B Gene as a Deletion Target in Cervical Cancer Cancer Research. 60: 6677-6682
Gaudray P, Carle GF, Gerhard DS, et al. (1999) Report of the Sixth International Workshop on Human Chromosome 11 Mapping 1998. Nice, France, May 2-5, 1998 Cytogenetics and Cell Genetics. 86: 167-186
Wlodarska I, Selleri L, Starza RL, et al. (1999) Molecular cytogenetics localizes two new breakpoints on 11q23.3 and 21q11.2 in myelodysplastic syndrome with t(11;21) translocation. Genes, Chromosomes and Cancer. 24: 199-206
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