Literature DB >> 1347397

Expansion of unstable DNA region in Japanese myotonic dystrophy patients.

H Yamagata, T Miki, T Ogihara, M Nakagawa, I Higuchi, M Osame, P Shelbourne, J Davies, K Johnson.   

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Year:  1992        PMID： 1347397     DOI： 10.1016/0140-6736(92)90862-w

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  12 in total

1.  Instability versus predictability: the molecular diagnosis of myotonic dystrophy.

Authors:  G K Suthers; S M Huson; K E Davies
Journal:  J Med Genet       Date:  1992-11       Impact factor: 6.318

2.  Anatomy of a founder effect: myotonic dystrophy in Northeastern Quebec.

Authors:  Vania Yotova; Damian Labuda; Ewa Zietkiewicz; Dominik Gehl; Alan Lovell; Jean-François Lefebvre; Stéphane Bourgeois; Emilie Lemieux-Blanchard; Marcin Labuda; Hélène Vézina; Louis Houde; Marc Tremblay; Bruno Toupance; Evelyne Heyer; Thomas J Hudson; Claude Laberge
Journal:  Hum Genet       Date:  2005-05-10       Impact factor: 4.132

3.  Segregation distortion of the CTG repeats at the myotonic dystrophy locus.

Authors:  R Chakraborty; D N Stivers; R Deka; L M Yu; M D Shriver; R E Ferrell
Journal:  Am J Hum Genet       Date:  1996-07       Impact factor: 11.025

4.  Founder effect and prevalence of myotonic dystrophy in South Africans: molecular studies.

Authors:  A Goldman; A Krause; M Ramsay; T Jenkins
Journal:  Am J Hum Genet       Date:  1996-08       Impact factor: 11.025

5.  Myotonic dystrophy: size- and sex-dependent dynamics of CTG meiotic instability, and somatic mosaicism.

Authors:  C Lavedan; H Hofmann-Radvanyi; P Shelbourne; J P Rabes; C Duros; D Savoy; I Dehaupas; S Luce; K Johnson; C Junien
Journal:  Am J Hum Genet       Date:  1993-05       Impact factor: 11.025

6.  Association of CTG repeats and the 1-kb Alu insertion/deletion polymorphism at the myotonin protein kinase gene in the Japanese population suggests a common Eurasian origin of the myotonic dystrophy mutation.

Authors:  H Yamagata; T Miki; M Nakagawa; K Johnson; R Deka; T Ogihara
Journal:  Hum Genet       Date:  1996-02       Impact factor: 4.132

7.  French myotonic dystrophy families show expansion of a CTG repeat in complete linkage disequilibrium with an intragenic 1 kb insertion.

Authors:  C Lavedan; H Hofmann-Radvanyi; C Boileau; C Bonaïti-Pellié; D Savoy; P Shelbourne; C Duros; J P Rabes; I Dehaupas; S Luce
Journal:  J Med Genet       Date:  1994-01       Impact factor: 6.318

8.  New founder haplotypes at the myotonic dystrophy locus in southern Africa.

Authors:  A Goldman; M Ramsay; T Jenkins
Journal:  Am J Hum Genet       Date:  1995-06       Impact factor: 11.025

9.  Comparison of the myotonic dystrophy associated CTG repeat in European and Japanese populations.

Authors:  J Davies; H Yamagata; P Shelbourne; J Buxton; T Ogihara; P Nokelainen; M Nakagawa; R Williamson; K Johnson; T Miki
Journal:  J Med Genet       Date:  1992-11       Impact factor: 6.318

10.  De novo myotonic dystrophy mutation in a Nigerian kindred.

Authors:  R Krahe; M Eckhart; A O Ogunniyi; B O Osuntokun; M J Siciliano; T Ashizawa
Journal:  Am J Hum Genet       Date:  1995-05       Impact factor: 11.025
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