Literature DB >> 1479600

Linkage investigation of three putative tuberous sclerosis determining loci on chromosomes 9q, 11q, and 12q. The Tuberous Sclerosis Collaborative Group.

J R Sampson1, L A Janssen, L A Sandkuijl.   

Abstract

Previous linkage studies in tuberous sclerosis have implicated three disease determining loci at 9q, 11q, and 12q. We have collated phenotypic and genotypic data on 1622 members of 128 families with tuberous sclerosis in order to evaluate simultaneously the evidence for these putative loci. Affection status in the family members has been reassessed using uniform diagnostic criteria and genotypic data extensively checked before analysis under alternative models of locus heterogeneity. One tuberous sclerosis determining locus, accounting for approximately 50% of the families studied, has been found to map in the region of D9S10 on 9q34 but no evidence has been found to support the existence of major loci on 11q or 12q. A locus, or loci, elsewhere in the genome is likely to account for tuberous sclerosis in most non-chromosome 9 linked families.

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Year:  1992        PMID: 1479600      PMCID: PMC1016202          DOI: 10.1136/jmg.29.12.861

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  24 in total

1.  Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I).

Authors:  P F Chance; T D Bird; P O'Connell; H Lipe; J M Lalouel; M Leppert
Journal:  Am J Hum Genet       Date:  1990-12       Impact factor: 11.025

2.  A comparative study on genetic heterogeneity in tuberous sclerosis: evidence for one gene on 9q34 and a second gene on 11q22-23.

Authors:  L A Janssen; S Povey; J Attwood; L A Sandkuyl; D Lindhout; P Flodman; M Smith; J R Sampson; J L Haines; E C Merkens
Journal:  Ann N Y Acad Sci       Date:  1991       Impact factor: 5.691

3.  A mapped set of genetic markers for human chromosome 9.

Authors:  M Lathrop; Y Nakamura; P O'Connell; M Leppert; S Woodward; J M Lalouel; R White
Journal:  Genomics       Date:  1988-11       Impact factor: 5.736

4.  Linkage analysis and family classification under heterogeneity.

Authors:  J Ott
Journal:  Ann Hum Genet       Date:  1983-10       Impact factor: 1.670

5.  Extensions to pedigree analysis. V. Optimal calculation of Mendelian likelihoods.

Authors:  K Lange; M Boehnke
Journal:  Hum Hered       Date:  1983       Impact factor: 0.444

6.  Absence of linkage of ABO blood group locus to familial tuberous sclerosis.

Authors:  R S Kandt; M A Pericak-Vance; W Y Hung; R J Gardner; M Nellist; K Phillips; K Warner; M C Speer; P E Crossen; N G Laing
Journal:  Exp Neurol       Date:  1989-06       Impact factor: 5.330

7.  A third gene locus for tuberous sclerosis is closely linked to the phenylalanine hydroxylase gene locus.

Authors:  R Fahsold; H D Rott; P Lorenz
Journal:  Hum Genet       Date:  1991-11       Impact factor: 4.132

8.  Evidence that the gene for tuberous sclerosis is on chromosome 9.

Authors:  A E Fryer; A Chalmers; J M Connor; I Fraser; S Povey; A D Yates; J R Yates; J P Osborne
Journal:  Lancet       Date:  1987-03-21       Impact factor: 79.321

9.  Tuberous sclerosis in a child with de novo translocation t(3;12) (p26.3;q23.3).

Authors:  R Fahsold; H D Rott; U Claussen; B Schmalenberger
Journal:  Clin Genet       Date:  1991-10       Impact factor: 4.438

10.  Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

Authors:  J D Brook; M E McCurrach; H G Harley; A J Buckler; D Church; H Aburatani; K Hunter; V P Stanton; J P Thirion; T Hudson
Journal:  Cell       Date:  1992-02-21       Impact factor: 41.582

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  5 in total

1.  Computer simulation of linkage and heterogeneity in tuberous sclerosis: a critical evaluation of the collaborative family data.

Authors:  L A Janssen; L A Sandkuijl; J R Sampson; D J Halley
Journal:  J Med Genet       Date:  1992-12       Impact factor: 6.318

2.  Inactivation of the cyclin-dependent kinase inhibitor p27 upon loss of the tuberous sclerosis complex gene-2.

Authors:  T Soucek; R S Yeung; M Hengstschläger
Journal:  Proc Natl Acad Sci U S A       Date:  1998-12-22       Impact factor: 11.205

Review 3.  Comprehensive mutation analysis of TSC1 and TSC2-and phenotypic correlations in 150 families with tuberous sclerosis.

Authors:  A C Jones; M M Shyamsundar; M W Thomas; J Maynard; S Idziaszczyk; S Tomkins; J R Sampson; J P Cheadle
Journal:  Am J Hum Genet       Date:  1999-05       Impact factor: 11.025

4.  Incorrect specification of marker allele frequencies: effects on linkage analysis.

Authors:  N B Freimer; L A Sandkuijl; S M Blower
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025

5.  Refined localization of TSC1 by combined analysis of 9q34 and 16p13 data in 14 tuberous sclerosis families.

Authors:  B Janssen; J Sampson; M van der Est; W Deelen; S Verhoef; I Daniels; A Hesseling; P Brook-Carter; M Nellist; D Lindhout
Journal:  Hum Genet       Date:  1994-10       Impact factor: 4.132

  5 in total

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