Literature DB >> 7977344

Refinement of the cone-rod retinal dystrophy locus on chromosome 19q.

C Y Gregory, K Evans, J L Whittaker, A Fryer, J Weissenbach, S S Bhattacharya.   

Abstract

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Year:  1994        PMID： 7977344      PMCID： PMC1918322     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  10 in total

1.  cDNA and genomic cloning of HRC, a human sarcoplasmic reticulum protein, and localization of the gene to human chromosome 19 and mouse chromosome 7.

Authors:  S L Hofmann; M Topham; C L Hsieh; U Francke
Journal:  Genomics       Date:  1991-04       Impact factor: 5.736

2.  A first-generation physical map of the human genome.

Authors:  D Cohen; I Chumakov; J Weissenbach
Journal:  Nature       Date:  1993-12-16       Impact factor: 49.962

3.  Evidence for human meiotic recombination interference obtained through construction of a short tandem repeat-polymorphism linkage map of chromosome 19.

Authors:  J L Weber; Z Wang; K Hansen; M Stephenson; C Kappel; S Salzman; P J Wilkie; B Keats; N C Dracopoli; B F Brandriff
Journal:  Am J Hum Genet       Date:  1993-11       Impact factor: 11.025

4.  Cone-rod retinal dystrophy in a patient with neurofibromatosis type 1.

Authors:  J A Kylstra; A S Aylsworth
Journal:  Can J Ophthalmol       Date:  1993-04       Impact factor: 1.882

5.  A procedure for combining two-point lod scores into a summary multipoint map.

Authors:  D Curtis; H Gurling
Journal:  Hum Hered       Date:  1993 May-Jun       Impact factor: 0.444

6.  Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19.

Authors:  M al-Maghtheh; C F Inglehearn; T J Keen; K Evans; A T Moore; M Jay; A C Bird; S S Bhattacharya
Journal:  Hum Mol Genet       Date:  1994-02       Impact factor: 6.150

7.  Physical and genetic characterization of the distal segment of the myotonic dystrophy area on 19q.

Authors:  G Jansen; P J de Jong; C Amemiya; C Aslanidis; D J Shaw; H G Harley; J D Brook; R Fenwick; R G Korneluk; C Tsilfidis
Journal:  Genomics       Date:  1992-07       Impact factor: 5.736

8.  Ocular changes in myotonic dystrophy.

Authors:  H M Burian; C A Burns
Journal:  Am J Ophthalmol       Date:  1967-01       Impact factor: 5.258

9.  Genetic linkage of cone-rod retinal dystrophy to chromosome 19q and evidence for segregation distortion.

Authors:  K Evans; A Fryer; C Inglehearn; J Duvall-Young; J L Whittaker; C Y Gregory; R Butler; N Ebenezer; D M Hunt; S Bhattacharya
Journal:  Nat Genet       Date:  1994-02       Impact factor: 38.330

10.  Deletion mapping of a retinal cone-rod dystrophy: assignment to 18q211.

Authors:  M Warburg; O Sjö; L Tranebjaerg; H C Fledelius
Journal:  Am J Med Genet       Date:  1991-06-01
  10 in total
  2 in total

1.  A new family of Greek origin maps to the CRD locus for autosomal dominant cone-rod dystrophy on 19q.

Authors:  M Papaioannou; D Bessant; A Payne; J Bellingham; C Rougas; A Loutradis-Anagnostou; C Gregory-Evans; A Balassopoulou; S Bhattacharya
Journal:  J Med Genet       Date:  1998-05       Impact factor: 6.318

2.  Microsatellite markers for the cone-rod retinal dystrophy gene, CRX, on 19q13.3.

Authors:  J Bellingham; C Y Gregory-Evans; K Gregory-Evans
Journal:  J Med Genet       Date:  1998-06       Impact factor: 6.318
  2 in total

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