Dinucleotide repeat polymorphisms at the D17S250 and D17S261 loci.

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

Who cites it

41 citing papers in PubMed.

1. Correlations between clinical, electrophysiological and genetic findings in hereditary motor and sensory neuropathy type I (HMSN I).Pflugers Archiv : European journal of physiology · 1996
   Trial
2. Low level microsatellite instability may be associated with reduced cancer specific survival in sporadic stage C colorectal carcinoma.Gut · 2005
   Article
3. Evidence for a cluster of genes on chromosome 17q11-q21 controlling susceptibility to tuberculosis and leprosy in Brazilians.Genes and immunity · 2004
   Article
4. An unconditional exact test for the Hardy-Weinberg equilibrium law: sample-space ordering using the Bayes factor.Genetics · 2001
   Article
5. A comparison of methods for gene dosage analysis in HMSN type 1.Journal of medical genetics · 2001
   Article
6. Combination analysis of genetic alterations and cell proliferation in small intestinal carcinomas.Digestive diseases and sciences · 2000
   Article
7. Toward a survey of somatic mutation of the NF1 gene in benign neurofibromas of patients with neurofibromatosis type 1.American journal of human genetics · 2000
   Article
8. A search for evidence of somatic mutations in the NF1 gene.Journal of medical genetics · 2000
   Article
9. Infrequent loss of heterozygosity of APC/MCC and DCC genes in gastric cancer showing DNA microsatellite instability.Journal of clinical pathology · 1999
   Article
10. Constitutional and mosaic large NF1 gene deletions in neurofibromatosis type 1.Journal of medical genetics · 1998
    Article
11. Low frequency of BRCA1 germline mutations in 45 German breast/ovarian cancer families.Journal of medical genetics · 1997
    Article
12. Immunogenetics of leishmanial and mycobacterial infections: the Belem Family Study.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 1997
    Review
13. Low Frequency Loss of Heterozygosity in the BRCA1 Region in Japanese Sporadic Breast Cancer.Breast cancer (Tokyo, Japan) · 1996
    Article
14. Colorectal neoplasms detected colonoscopically in at-risk members of colorectal cancer families stratified by the demonstration of DNA microsatellite instability.Journal of molecular medicine (Berlin, Germany) · 1996
    Article
15. Allelic imbalance in the region of the BRCA1 gene in ductal carcinoma in situ of the breast.British journal of cancer · 1996
    Article
16. Molecular genetic analysis of the 17p11.2 region in patients with hereditary neuropathy with liability to pressure palsies (HNPP).Human genetics · 1996
    Article
17. A de novo satellited short arm of the Y chromosome possibly resulting from an unstable translocation.Human genetics · 1995
    Article
18. Frequent genetic instability in small intestinal carcinomas.Japanese journal of cancer research : Gann · 1995
    Article
19. Loss of heterozygosity in lobular carcinoma in situ of the breast.Clinical molecular pathology · 1995
    Article
20. An evaluation of genetic heterogeneity in 145 breast-ovarian cancer families. Breast Cancer Linkage Consortium.American journal of human genetics · 1995
    Article

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

Authors and funding

6 authors.

Funding

Abstract

PubMed holds no abstract for this paper.

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