Literature DB >> 2017388

Dinucleotide repeat polymorphism at the GSN locus (9q32-34).

D J Kwiatkowski1, S Perman.   

Abstract

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Year:  1991        PMID： 2017388      PMCID： PMC333757     

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


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  1 in total

1.  Localization of gelsolin proximal to ABL on chromosome 9.

Authors:  D J Kwiatkowski; C A Westbrook; G A Bruns; C C Morton
Journal:  Am J Hum Genet       Date:  1988-04       Impact factor: 11.025
  1 in total
  10 in total

1.  Evidence for genetic heterogeneity in tuberous sclerosis: one locus on chromosome 9 and at least one locus elsewhere.

Authors:  H Northrup; D J Kwiatkowski; E S Roach; W B Dobyns; R A Lewis; G E Herman; E Rodriguez; S P Daiger; S H Blanton
Journal:  Am J Hum Genet       Date:  1992-10       Impact factor: 11.025

2.  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

3.  Identification of markers flanking the tuberous sclerosis locus on chromosome 9 (TSC1).

Authors:  M Nellist; P T Brook-Carter; J M Connor; D J Kwiatkowski; P Johnson; J R Sampson
Journal:  J Med Genet       Date:  1993-03       Impact factor: 6.318

4.  Late onset lattice corneal dystrophy with systemic familial amyloidosis, amyloidosis V, in an English family.

Authors:  H S Stewart; R Parveen; A E Ridgway; R Bonshek; G C Black
Journal:  Br J Ophthalmol       Date:  2000-04       Impact factor: 4.638

5.  Individual DNA identification from ancient human remains.

Authors:  K Kurosaki; T Matsushita; S Ueda
Journal:  Am J Hum Genet       Date:  1993-09       Impact factor: 11.025

6.  Localization of one gene for tuberous sclerosis within 9q32-9q34, and further evidence for heterogeneity.

Authors:  J L Haines; M P Short; D J Kwiatkowski; A Jewell; E Andermann; B Bejjani; C H Yang; J F Gusella; J A Amos
Journal:  Am J Hum Genet       Date:  1991-10       Impact factor: 11.025

7.  Torsion dystonia genes in two populations confined to a small region on chromosome 9q32-34.

Authors:  D J Kwiatkowski; L Ozelius; P L Kramer; S Perman; D E Schuback; J F Gusella; S Fahn; X O Breakefield
Journal:  Am J Hum Genet       Date:  1991-08       Impact factor: 11.025

8.  Linkage analysis of the nail-patella syndrome.

Authors:  E Campeau; D Watkins; G A Rouleau; R Babul; J A Buchanan; W Meschino; V M Der Kaloustian
Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025

9.  Exclusion of the gelsolin gene on 9q32-34 as the cause of familial lattice corneal dystrophy type I.

Authors:  A Wiens; S Marles; J Safneck; D J Kwiatkowski; C P Maury; T Zelinski; S Philipps; M B Ekins; C R Greenberg
Journal:  Am J Hum Genet       Date:  1992-07       Impact factor: 11.025

10.  Asp187Asn mutation of gelsolin in an American kindred with familial amyloidosis, Finnish type (FAP IV).

Authors:  R D Steiner; T Paunio; T Uemichi; J P Evans; M D Benson
Journal:  Hum Genet       Date:  1995-03       Impact factor: 4.132
  10 in total

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