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32199 publications found in the database

2007 (3910)

*Starting in 2010, coverage has been refocused on core journals.

2007 Publications

Genome-wide analysis of DNA copy number changes and LOH in CLL using high-density SNP arrays
Pfeifer, D. et al. Blood 109(3), 1202-10, 2007  PubMed

Sequence variant in the laminin gamma1 (LAMC1) gene associated with familial pelvic organ prolapse
Nikolova, G. et al. Human Genetics 120(6), 847-56, 2007  PubMed

Admixture in Mexico City: implications for admixture mapping of type 2 diabetes genetic risk factors
Martinez-Marignac, V. L. et al. Human Genetics 120(6), 807-19, 2007  PubMed

High-resolution analysis of allelic imbalance in neuroblastoma cell lines by single nucleotide polymorphism arrays
Carr, J. et al. Cancer Genetics and Cytogenetics 172(2), 127-38, 2007  PubMed

The South African "bathing suit ichthyosis" is a form of lamellar ichthyosis caused by a homozygous missense mutation, p.R315L, in transglutaminase 1
Arita, K. et al. Journal of Investigative Dermatology 127(2), 490-3, 2007  PubMed

Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia
Tekin, M. et al. American Journal of Human Genetics 80(2), 338-44, 2007  PubMed

Genome-wide linkage scan for breast cancer susceptibility loci in Swedish hereditary non-BRCA1/2 families: Suggestive linkage to 10q23.31-q25.3
Bergman, A. et al. Genes Chromosomes & Cancer 46(3), 302-9, 2007  PubMed

Assignment of the gene locus for severe congenital neutropenia to chromosome 1q22 in the original Kostmann family from Northern Sweden
Melin, M. et al. Biochemical and Biophysical Research Communications 353(3), 571-5, 2007  PubMed

Autozygosity mapping of Bardet-Biedl syndrome to 12q21.2 and confirmation of FLJ23560 as BBS10
White, D. R. A. et al. European Journal of Human Genetics 15(2), 173-8, 2007  PubMed

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