Literature DB >> 2020562

Dinucleotide repeat polymorphism at the D6S109 locus.

L P Ranum1, M Y Chung, L A Duvick, H Y Zoghbi, H T Orr.   

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Year:  1991        PMID： 2020562      PMCID： PMC333832          DOI： 10.1093/nar/19.5.1171-a

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN： 0305-1048            Impact factor:   16.971


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  1 in total

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  1 in total
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1.  Nonsyndromic cleft lip and palate: evidence of linkage to a microsatellite marker on 6p23.

Authors:  F Carinci; F Pezzetti; L Scapoli; E Padula; U Baciliero; C Curioni; M Tognon
Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025

2.  Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15.

Authors:  E L Grigorenko; F B Wood; M S Meyer; L A Hart; W C Speed; A Shuster; D L Pauls
Journal:  Am J Hum Genet       Date:  1997-01       Impact factor: 11.025

3.  The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locus.

Authors:  T J Kwiatkowski; H T Orr; S Banfi; A E McCall; C Jodice; F Persichetti; A Novelletto; F LeBorgne-DeMarquoy; L A Duvick; M Frontali
Journal:  Am J Hum Genet       Date:  1993-08       Impact factor: 11.025

4.  Localization of the hemochromatosis gene close to D6S105.

Authors:  E C Jazwinska; S C Lee; S I Webb; J W Halliday; L W Powell
Journal:  Am J Hum Genet       Date:  1993-08       Impact factor: 11.025

5.  Molecular heterogeneity of autosomal dominant cerebellar ataxia: analysis of flanking microsatellites of the spinocerebellar ataxia 1 locus in a northern European family unequivocally demonstrates non-linkage.

Authors:  A Lunkes; S Gispert; J Enczmann; G Auburger
Journal:  Hum Genet       Date:  1993-05       Impact factor: 4.132

6.  Linkage analysis of idiopathic generalized epilepsy (IGE) and marker loci on chromosome 6p in families of patients with juvenile myoclonic epilepsy: no evidence for an epilepsy locus in the HLA region.

Authors:  W P Whitehouse; M Rees; D Curtis; A Sundqvist; K Parker; E Chung; D Baralle; R M Gardiner
Journal:  Am J Hum Genet       Date:  1993-09       Impact factor: 11.025

7.  Autosomal dominant retinitis pigmentosa (adRP; RP6): cosegregation of RP6 and the peripherin-RDS locus in a late-onset family of Irish origin.

Authors:  S A Jordan; G J Farrar; R Kumar-Singh; P Kenna; M M Humphries; V Allamand; E M Sharp; P Humphries
Journal:  Am J Hum Genet       Date:  1992-03       Impact factor: 11.025

8.  Frequent loss of heterozygosity on chromosome 6 in human ovarian carcinoma.

Authors:  W D Foulkes; J Ragoussis; G W Stamp; G J Allan; J Trowsdale
Journal:  Br J Cancer       Date:  1993-03       Impact factor: 7.640

9.  High relative frequency of SCA1 in Poland reflecting a potential founder effect.

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Journal:  Neurol Sci       Date:  2016-05-19       Impact factor: 3.307
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