Literature DB >> 8244374

A high-resolution linkage map of human 9q34.1.

E P Henske1, L Ozelius, J F Gusella, J L Haines, D J Kwiatkowski.   

Abstract

A map comprising 16 distinct markers with heterozygosities of 0.61-0.92 for a 10-cM region of human 9q34.1 is presented. The map incorporates four genes and has a maximum intermarker interval of 2.1 cM. Markers were analyzed in the Venezuelan reference pedigrees and all were placed uniquely in the map with a minimum likelihood of 676:1. The map should prove useful in analysis of families segregating dystonia and tuberous sclerosis, as the DYT1 and TSC1 loci map within this region.

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Year:  1993        PMID： 8244374     DOI： 10.1006/geno.1993.1376

Source DB:  PubMed          Journal:  Genomics        ISSN： 0888-7543            Impact factor:   5.736


  8 in total

1.  Loss of heterozygosity on chromosomes 9q and 16p in atypical adenomatous hyperplasia concomitant with adenocarcinoma of the lung.

Authors:  K Takamochi; T Ogura; K Suzuki; H Kawasaki; Y Kurashima; T Yokose; A Ochiai; K Nagai; Y Nishiwaki; H Esumi
Journal:  Am J Pathol       Date:  2001-11       Impact factor: 4.307

2.  Tuberous sclerosis-associated renal cell carcinoma. Clinical, pathological, and genetic features.

Authors:  J Bjornsson; M P Short; D J Kwiatkowski; E P Henske
Journal:  Am J Pathol       Date:  1996-10       Impact factor: 4.307

3.  Allelic loss is frequent in tuberous sclerosis kidney lesions but rare in brain lesions.

Authors:  E P Henske; B W Scheithauer; M P Short; R Wollmann; J Nahmias; N Hornigold; M van Slegtenhorst; C T Welsh; D J Kwiatkowski
Journal:  Am J Hum Genet       Date:  1996-08       Impact factor: 11.025

4.  Evidence that lymphangiomyomatosis is caused by TSC2 mutations: chromosome 16p13 loss of heterozygosity in angiomyolipomas and lymph nodes from women with lymphangiomyomatosis.

Authors:  T A Smolarek; L L Wessner; F X McCormack; J C Mylet; A G Menon; E P Henske
Journal:  Am J Hum Genet       Date:  1998-04       Impact factor: 11.025

5.  Linkage of hereditary haemorrhagic telangiectasia to chromosome 9q34 and evidence for locus heterogeneity.

Authors:  P Heutink; T Haitjema; G J Breedveld; B Janssen; L A Sandkuijl; C J Bontekoe; C J Westerman; B A Oostra
Journal:  J Med Genet       Date:  1994-12       Impact factor: 6.318

6.  The DYT1 gene on 9q34 is responsible for most cases of early limb-onset idiopathic torsion dystonia in non-Jews.

Authors:  P L Kramer; G A Heiman; T Gasser; L J Ozelius; D de Leon; M F Brin; R E Burke; J Hewett; A L Hunt; C Moskowitz
Journal:  Am J Hum Genet       Date:  1994-09       Impact factor: 11.025

7.  Adult onset idiopathic torsion dystonia is excluded from the DYT 1 region (9q34) in a Swedish family.

Authors:  G Holmgren; L Ozelius; L Forsgren; B G Almay; M Holmberg; P Kramer; S Fahn; X O Breakefield
Journal:  J Neurol Neurosurg Psychiatry       Date:  1995-08       Impact factor: 10.154

8.  Gene expression profiling of lymphoblastoid cell lines from monozygotic twins discordant in severity of autism reveals differential regulation of neurologically relevant genes.

Authors:  Valerie W Hu; Bryan C Frank; Shannon Heine; Norman H Lee; John Quackenbush
Journal:  BMC Genomics       Date:  2006-05-18       Impact factor: 3.969
  8 in total

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