Home LiteratureArticle Details
PMID: 2491780 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Linkage analysis of chromosome 17 markers in British and South African families with neurofibromatosis type I.

American journal of human genetics ·Vol. 44 ·No. 1 ·1989-01-00 ·Pages 38-40

Mathew CG, Thorpe K, Easton DF, Chin KS, Jadayel D, Ponder M, Moore G, Wallis CE, Slater CP, De Jong G

Abstract

Nine markers from the pericentromeric region of chromosome 17 were typed in 16 British and five South African families with neurofibromatosis type 1 (NF1). The markers--p17H8, pHHH202, and EW204--were linked to NF1 at recombination fractions less than 1%. No evidence of locus heterogeneity was detected. Inspection of recombinant events in families informative for several markers suggests that the NF1 gene is located between the markers EW301 (cen-p11.2) and EW206 (cen-q12) and possibly distal to pHHH202 (q11.2-q12).

MeSH Terms
Chromosomes, Human, Pair 17 Female Genetic Linkage Genetic Markers Humans Male Neurofibromatosis 1/genetics South Africa United Kingdom
Chemicals
Genetic Markers
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Mathew C G
Section of Human Cancer Genetics, Institute of Cancer Research, Surrey, United Kingdom.
Thorpe K
Easton D F
Chin K S
Jadayel D
Ponder M
Moore G
Wallis C E
Slater C P
De Jong G
References (13)
13 references, click to expand
  1. Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17.
    Science. 1987 May 29;236(4805):1100-2 PMID: 3107130
  2. Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene.
    Cell. 1987 Jun 5;49(5):589-94 PMID: 2884037
  3. Neurofibromatosis in the South African Indian community--further evidence for heterogeneity?
    S Afr Med J. 1987 Oct 3;72(7):478-80 PMID: 3116684
  4. Multipoint linkage analysis in neurofibromatosis type I: an international collaboration.
    Am J Hum Genet. 1989 Jan;44(1):6-12 PMID: 2491784
  5. Characterization of a panel of highly variable minisatellites cloned from human DNA.
    Ann Hum Genet. 1987 Oct;51(Pt 4):269-88 PMID: 3482146
  6. Genetic analysis of NF1: identification of close flanking markers on chromosome 17.
    Genomics. 1987 Dec;1(4):340-5 PMID: 3130304
  7. RFLP for the human erb-A1 gene.
    Nucleic Acids Res. 1987 Jan 26;15(2):863 PMID: 2881264
  8. Regional mapping panel for human chromosome 17: application to neurofibromatosis type 1.
    Genomics. 1987 Dec;1(4):374-81 PMID: 3130306
  9. Linkage of NF1 to 12 chromosome 17 markers: a summary of eight concurrent reports.
    Genomics. 1987 Dec;1(4):382-3 PMID: 2896634
  10. Linkage analysis of British and Indian families with Von Recklinghausen neurofibromatosis.
    J Med Genet. 1987 Sep;24(9):524-6 PMID: 3118029
  11. Multilocus linkage analysis in humans: detection of linkage and estimation of recombination.
    Am J Hum Genet. 1985 May;37(3):482-98 PMID: 3859205
  12. Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: implications for development of centromere-based genetic linkage maps.
    Proc Natl Acad Sci U S A. 1986 Aug;83(15):5611-5 PMID: 3016709
  13. Tightly linked markers for the neurofibromatosis type 1 gene.
    Genomics. 1987 Dec;1(4):364-7 PMID: 2896632
Article Info
Journal
American journal of human genetics
Abbr.
Am J Hum Genet
ISSN
0002-9297
Published
1989-01-00
Pages
38-40
Language
English
Region
United States
NLM ID
0370475
PMCID
PMC1715463
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com