Revised 14.7-cM locus for the hyperparathyroidism-jaw tumor syndrome gene, HRPT2
- PMID: 11951180
- PMCID: PMC447614
- DOI: 10.1086/340093
Revised 14.7-cM locus for the hyperparathyroidism-jaw tumor syndrome gene, HRPT2
References
Electronic-Database Information
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- GenBank, http://www.ncbi.nlm.nih.gov/Genbank/ (for marker 277P6-2A8 [accession number AF181675])
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- Généthon, http://www.genethon.fr/
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- Human Genome Working Draft, http://genome.ucsc.edu/ (for the sequence from D1S240 to D1S477, estimated at 17.5 Mb)
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- Online Mendelian Inheritance in Man (OMIM), http://www.ncbi.nlm.nih.gov/Omim/ (for hyperparathyroidism–jaw tumor syndrome [MIM 145001])
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- Whitehead Institute for Genome Research, http://www-genome.wi.mit.edu/
References
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- Carpten JD, Makalowska I, Robbins CM, Scott N, Sood R, Connors TD, Bonner TI, Smith JR, Faruque MU, Stephan DA, Pinkett H, Morgenbesser SD, Su K, Graham C, Gregory SG, Williams H, McDonald L, Baxevanis AD, Klingler KW, Landes GM, Trent JM (2000) A 6-Mb high-resolution physical and transcription map encompassing the hereditary prostate cancer 1 (HPC1) region. Genomics 64:1–14 - PubMed
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- Dib C, Faure S, Fizames C, Samson D, Drouot N, Vignal A, Millasseau P, Marc S, Hazan J, Seboun E, Lathrop M, Gyapay G, Morissette J, Weissenbach J (1996) A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 380:152–154 - PubMed
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- Donoso LA, Frost AT, Stone EM, Weleber RG, MacDonald IM, Hageman GS, Cibis GW, Ritter R III, Edwards AO (2001) Autosomal dominant Stargardt-like macular dystrophy: founder effect and reassessment of genetic heterogeneity. Arch Ophthalmol 119:564–570 - PubMed
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