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A high-resolution STS, EST, and gene-based physical map of the hereditary paraganglioma region on chromosome 11q23.
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Familial paragangliomas: linkage to chromosome 11q23 and clinical implications.
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Rare disease genes--lessons and challenges.
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Genetic predisposition to phaeochromocytoma: analysis of candidate genes GDNF, RET and VHL.
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A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families.
Am J Hum Genet. 1997 May;60(5):1041-9.
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Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23.
Am J Hum Genet. 1997 Jan;60(1):121-32.
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Confinement of PGL, an imprinted gene causing hereditary paragangliomas, to a 2-cM interval on 11q22-q23 and exclusion of DRD2 and NCAM as candidate genes.
Eur J Hum Genet. 1996;4(5):267-73. doi: 10.1159/000472213.
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First experiences with genetic counselling based on predictive DNA diagnosis in hereditary glomus tumours (paragangliomas).
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Genetic mapping using haplotype, association and linkage methods suggests a locus for severe bipolar disorder (BPI) at 18q22-q23.
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A comprehensive genetic map of the human genome based on 5,264 microsatellites.
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