Literature DB >> 1923786

Dinucleotide repeat polymorphisms at the DXS294 and DXS300 loci in Xq26.

A K Gedeon1, R I Richards, J C Mulley.   

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Year:  1991        PMID： 1923786      PMCID： PMC328826          DOI： 10.1093/nar/19.18.5087

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


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  3 in total

1.  Fragile X syndrome: diagnosis using highly polymorphic microsatellite markers.

Authors:  R I Richards; Y Shen; K Holman; H Kozman; V J Hyland; J C Mulley; G R Sutherland
Journal:  Am J Hum Genet       Date:  1991-06       Impact factor: 11.025

2.  Predictive diagnosis of myotonic dystrophy with flanking microsatellite markers.

Authors:  J C Mulley; A K Gedeon; S J White; E A Haan; R I Richards
Journal:  J Med Genet       Date:  1991-07       Impact factor: 6.318

3.  Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines.

Authors:  G K Suthers; V J Hyland; D F Callen; I Oberle; M Rocchi; N S Thomas; C P Morris; C E Schwartz; M Schmidt; H H Ropers
Journal:  Am J Hum Genet       Date:  1990-08       Impact factor: 11.025
  3 in total
  2 in total

1.  Linkage mapping of a severe X-linked mental retardation syndrome.

Authors:  H Malmgren; M Sundvall; N Dahl; K H Gustavson; G Annerén; C Wadelius; M L Steén-Bondeson; U Pettersson
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025

2.  X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome.

Authors:  A K Gedeon; M J Wilson; A C Colley; D O Sillence; J C Mulley
Journal:  J Med Genet       Date:  1995-05       Impact factor: 6.318
  2 in total

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