Literature DB >> 8818958

Still no evidence for heterogeneity in Best's vitelliform macular dystrophy.

C Graff, C Wadelius.   

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Year:  1996        PMID： 8818958      PMCID： PMC1050686          DOI： 10.1136/jmg.33.7.630

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  6 in total

1.  Fine mapping of Best's macular dystrophy localizes the gene in close proximity to but distinct from the D11S480/ROM1 loci.

Authors:  C Graff; K Forsman; C Larsson; S Nordström; L Lind; K Johansson; O Sandgren; J Weissenbach; G Holmgren; K H Gustavson
Journal:  Genomics       Date:  1994-12       Impact factor: 5.736

2.  Best's vitelliform dystrophy (VMD2) maps between D11S903 and PYGM: no evidence for locus heterogeneity.

Authors:  B H Weber; D Walker; B Müller; L Mar
Journal:  Genomics       Date:  1994-03-15       Impact factor: 5.736

3.  The gene for Best's macular dystrophy is located at 11q13 in a Swedish family.

Authors:  K Forsman; C Graff; S Nordström; K Johansson; E Westermark; E Lundgren; K H Gustavson; C Wadelius; G Holmgren
Journal:  Clin Genet       Date:  1992-09       Impact factor: 4.438

4.  Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13.

Authors:  E M Stone; B E Nichols; L M Streb; A E Kimura; V C Sheffield
Journal:  Nat Genet       Date:  1992-07       Impact factor: 38.330

5.  Evidence for genetic heterogeneity in Best's vitelliform macular dystrophy.

Authors:  F C Mansergh; P F Kenna; G Rudolph; T Meitinger; G J Farrar; R Kumar-Singh; J Scorer; A M Hally; L Mynett-Johnson; M M Humphries
Journal:  J Med Genet       Date:  1995-11       Impact factor: 6.318

6.  A recombination event excludes the ROM1 locus from the Best's vitelliform macular dystrophy region.

Authors:  H Stöhr; B H Weber
Journal:  Hum Genet       Date:  1995-02       Impact factor: 4.132
  6 in total
  1 in total

1.  Lack of evidence for genetic heterogeneity in Best vitelliform macular dystrophy.

Authors:  F Mansergh; T Meitinger; G Rodolph; P Humphries; G J Farrar
Journal:  J Med Genet       Date:  1998-01       Impact factor: 6.318
  1 in total

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