Literature DB >> 8334899

Report and abstracts of the Second International Workshop on Human Chromosome 9 Mapping 1993.

D J Kwiatkowski1, J Armour, A E Bale, J W Fountain, D Goudie, J L Haines, M A Knowles, A Pilz, S Slaugenhaupt, S Povey.   

Abstract

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Year:  1993        PMID: 8334899     DOI: 10.1159/000133566

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN: 0301-0171


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  8 in total

1.  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

2.  Molecular analysis of the human vitamin D binding protein (group specific component, Gc) in tuberous sclerosis complex (TSC).

Authors:  J A Rodriguez; R L Evans; S P Daiger; H Northrup
Journal:  J Med Genet       Date:  1997-06       Impact factor: 6.318

3.  An index marker map of chromosome 9 provides strong evidence for positive interference.

Authors:  D J Kwiatkowski; C Dib; S A Slaugenhaupt; S Povey; J F Gusella; J L Haines
Journal:  Am J Hum Genet       Date:  1993-12       Impact factor: 11.025

4.  Construction of cosmid libraries from flow-sorted human chromosomes 1, 6, 7, 11, 13, and 18 for reference library resources.

Authors:  D Nizetic; S Monard; B Young; F Cotter; G Zehetner; H Lehrach
Journal:  Mamm Genome       Date:  1994-12       Impact factor: 2.957

5.  Genetic heterogeneity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotype.

Authors:  K A McAllister; F Lennon; B Bowles-Biesecker; W C McKinnon; E A Helmbold; D S Markel; C E Jackson; A E Guttmacher; M A Pericak-Vance; D A Marchuk
Journal:  J Med Genet       Date:  1994-12       Impact factor: 6.318

6.  Refined mapping of a gene responsible for Fukuyama-type congenital muscular dystrophy: evidence for strong linkage disequilibrium.

Authors:  T Toda; S Ikegawa; K Okui; E Kondo; K Saito; Y Fukuyama; M Yoshioka; T Kumagai; K Suzumori; I Kanazawa
Journal:  Am J Hum Genet       Date:  1994-11       Impact factor: 11.025

7.  Homozygous deletions on the short arm of chromosome 9 in ovarian adenocarcinoma cell lines and loss of heterozygosity in sporadic tumors.

Authors:  G Chenevix-Trench; J Kerr; M Friedlander; T Hurst; B Sanderson; M Coglan; B Ward; J Leary; S K Khoo
Journal:  Am J Hum Genet       Date:  1994-07       Impact factor: 11.025

8.  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

  8 in total

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