Literature DB >> 8098983

AK1 detects a VNTR locus in the pseudoautosomal region.

A Klink1, M Wapenaar, G J van Ommen, G Rappold.   

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Year:  1993        PMID： 8098983     DOI： 10.1093/hmg/2.3.339-a

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


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  2 in total

1.  A patient with an interstitial deletion in Xp22.3 locates the gene for X-linked recessive chondrodysplasia punctata to within a one megabase interval.

Authors:  A Klink; A Meindl; H Hellebrand; G A Rappold
Journal:  Hum Genet       Date:  1994-04       Impact factor: 4.132

2.  Identification of a major recombination hotspot in patients with short stature and SHOX deficiency.

Authors:  Katja U Schneider; Nitin Sabherwal; Karin Jantz; Ralph Röth; Nadja Muncke; Werner F Blum; Gordon B Cutler; Gudrun Rappold
Journal:  Am J Hum Genet       Date:  2005-06-01       Impact factor: 11.025
  2 in total

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