Linkage disequilibrium narrows locus for venous malformation with glomus cells (VMGLOM) to a single 1.48 Mbp YAC

European Journal of Human Genetics

Volumn 9, Issue 1, 2001, Pages 34-38

  Irrthum, Alexandre ^a   Brouillard, Pascal ^a   Enjolras, Odile ^b   Gibbs, Neil F ^c   Eichenfield, Lawrence F ^c   Olsen, Bjorn R ^d   Mulliken, John B ^e   Boon, Laurence M ^a,f   Vikkula, Miikka ^a  

^a DE DUVE INSTITUTE   (Belgium)

^b HÔPITAL LARIBOISIÈRE   (France)

^c RADY CHILDREN'S HOSPITAL   (United States)

^d HARVARD MEDICAL SCHOOL   (United States)

^e BOSTON CHILDREN S HOSPITAL   (United States)

^f CLINIQUES UNIVERSITAIRES SAINT LUC   (Belgium)

Author keywords

Chromosome 1p21 p22; Glomangioma; Haplotype sharing; Multiple glomus tumor; Vascular anomaly

Indexed keywords

ADOLESCENT; ALLELE; ANGIOGENESIS; ARTICLE; BLOOD VESSEL; CHILD; CHROMOSOME 1P; CLINICAL ARTICLE; CROSSING OVER; FAMILIAL DISEASE; FEMALE; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENE MAPPING; GENETIC LINKAGE; HAPLOTYPE; HUMAN; INHERITANCE; MALE; MORPHOGENESIS; POPULATION; PRIORITY JOURNAL; REGULATORY MECHANISM; SKIN DEFECT; VEIN MALFORMATION; YEAST ARTIFICIAL CHROMOSOME;

GLOMUS;

EID: 0035144571     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5200576     Document Type: Article

References (8)

1. Molecular basis of vascular anomalies
2. Hemangiomas and vascular malformations in infants and children: A classification based on endothelial characteristics
3. Assignment of a locus for dominantly inherited venous malformations to chromosome 9p
4. Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2
5. A gene for inherited cutaneous venous anomalies (′glomangiomas′) localizes to chromosome 1p21-22
6. High-resolution physical and transcript map of the locus for venous malformations with glomus cells (VMGLOM) on chromosome 1p21-p22
7. Strategies for multilocus linkage analysis in humans
8. Hereditary multiple glomangiomas