Literature DB >> 7902166

An NciI RFLP at the D15S63 locus in the critical Prader-Willi syndrome region in 15q11-13.

B Dittrich1, S Gross, K Buiting, B Horsthemke.   

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Year:  1993        PMID： 7902166     DOI： 10.1093/hmg/2.9.1509

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


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  4 in total

1.  Clonal heterogeneity at allelic methylation sites diagnostic for Prader-Willi and Angelman syndromes.

Authors:  J M LaSalle; R J Ritchie; H Glatt; M Lalande
Journal:  Proc Natl Acad Sci U S A       Date:  1998-02-17       Impact factor: 11.205

2.  An insertion/deletion polymorphism at the D15S63 locus in the critical Prader-Willi syndrome region in 15q11-13.

Authors:  B Dittrich; K Buiting; S Gross; B Horsthemke
Journal:  Hum Genet       Date:  1994-11       Impact factor: 4.132

3.  Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes.

Authors:  A Reis; B Dittrich; V Greger; K Buiting; M Lalande; G Gillessen-Kaesbach; M Anvret; B Horsthemke
Journal:  Am J Hum Genet       Date:  1994-05       Impact factor: 11.025

4.  Epimutations in Prader-Willi and Angelman syndromes: a molecular study of 136 patients with an imprinting defect.

Authors:  Karin Buiting; Stephanie Gross; Christina Lich; Gabriele Gillessen-Kaesbach; Osman el-Maarri; Bernhard Horsthemke
Journal:  Am J Hum Genet       Date:  2003-01-23       Impact factor: 11.025
  4 in total

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