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4 in total

1. Criteria for establishing the validity of genetic recombination in myotonic dystrophy.

Authors: R C Griggs; D S Wood
Journal: Neurology Date: 1989-03 Impact factor: 9.910

2. Gonosomal mosaicism in myotonic dystrophy patients: involvement of mitotic events in (CTG)n repeat variation and selection against extreme expansion in sperm.

Authors: G Jansen; P Willems; M Coerwinkel; W Nillesen; H Smeets; L Vits; C Höweler; H Brunner; B Wieringa
Journal: Am J Hum Genet Date: 1994-04 Impact factor: 11.025

3. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

Authors: J D Brook; M E McCurrach; H G Harley; A J Buckler; D Church; H Aburatani; K Hunter; V P Stanton; J P Thirion; T Hudson
Journal: Cell Date: 1992-02-21 Impact factor: 41.582

4. Origin of the expansion mutation in myotonic dystrophy.

Authors: G Imbert; C Kretz; K Johnson; J L Mandel
Journal: Nat Genet Date: 1993-05 Impact factor: 38.330

4 in total

2 in total

1. Replacement of the myotonic dystrophy type 1 CTG repeat with 'non-CTG repeat' insertions in specific tissues.

Authors: Michelle M Axford; Arturo López-Castel; Masayuki Nakamori; Charles A Thornton; Christopher E Pearson
Journal: J Med Genet Date: 2011-05-27 Impact factor: 6.318

2. High germinal instability of the (CTG)n at the SCA8 locus of both expanded and normal alleles.

Authors: I Silveira; I Alonso; L Guimarães; P Mendonça; C Santos; P Maciel; J M Fidalgo De Matos; M Costa; C Barbot; A Tuna; J Barros; L Jardim; P Coutinho; J Sequeiros
Journal: Am J Hum Genet Date: 2000-03 Impact factor: 11.025

2 in total