Literature DB >> 8111402

A CA-repeat polymorphism near DXS418 (P122).

E Van De Vosse1, P F Booms, R H Vossen, M C Wapenaar, G J Van Ommen, J T Den Dunnen.   

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Year:  1993        PMID： 8111402     DOI： 10.1093/hmg/2.12.2202-a

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN： 0964-6906            Impact factor:   6.150


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  4 in total

1.  Fried syndrome is a distinct X linked mental retardation syndrome mapping to Xp22.

Authors:  L Strain; A F Wright; D T Bonthron
Journal:  J Med Genet       Date:  1997-07       Impact factor: 6.318

2.  Improved genetic mapping of X linked retinoschisis.

Authors:  N D George; S J Payne; R M Bill; D E Barton; A T Moore; J R Yates
Journal:  J Med Genet       Date:  1996-11       Impact factor: 6.318

3.  Linkage disequilibrium and physical mapping of X-linked juvenile retinoschisis.

Authors:  L Huopaniemi; A Rantala; E Tahvanainen; A de la Chapelle; T Alitalo
Journal:  Am J Hum Genet       Date:  1997-05       Impact factor: 11.025

4.  High-resolution mapping by YAC fragmentation of a 2.5-Mb Xp22 region containing the human RS, KFSD and CLS disease genes.

Authors:  E Van de Vosse; P Van der Bent; J J Heus; G J Van Ommen; J T Den Dunnen
Journal:  Mamm Genome       Date:  1997-07       Impact factor: 2.957
  4 in total

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