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

European Journal of Human Genetics

Volumn 4, Issue 5, 1996, Pages 267-273

  Van Schothorst, Evert M ^a  

^a LEIDEN UNIVERSITY   (Netherlands)

Author keywords

Chromosome 11q22 q23; Glomus tumour; Haplotype sharing; Linkage; Paraganglioma

Indexed keywords

ARTICLE; CHROMOSOME 11Q; FRANCE; GENE MAPPING; GENETIC LINKAGE; GENETIC MARKER; HAPLOTYPE; HEAD AND NECK TUMOR; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; NETHERLANDS; PARAGANGLIOMA; PRIORITY JOURNAL;

GLOMUS;

EID: 0029862406     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1159/000472213     Document Type: Article

References (2)

1. Zak FG, Lawson W: The Paragangliomic Chemoreceptor System: Physiology, Pathology and Clinical Medicine. New York, Springer, 1982, p 583.
2. Van der Mey AGL, Maaswinkel-Mooy PD, Cornelisse CJ, Schmidt PH, van de Kamp JJP: Genomic imprinting in hereditary glomus tumors: Evidence for new genetic theory. Lancet 1989;ii:1291-1294.