139 related articles for article (PubMed ID: 7936256)
1. Congenital myotonic dystrophy transmitted from an asymptomatic father with a DM-specific gene.
Ohya K; Tachi N; Chiba S; Sato T; Kon S; Kikuchi K; Imamura S; Yamagata H; Miki T
Neurology; 1994 Oct; 44(10):1958-60. PubMed ID: 7936256
[TBL] [Abstract][Full Text] [Related]
2. Detection of the CTG repeat expansion in congenital myotonic dystrophy.
Ohya K; Tachi N; Sato T; Kon S; Kikuchi K; Chiba S
Jpn J Hum Genet; 1997 Mar; 42(1):169-80. PubMed ID: 9183996
[TBL] [Abstract][Full Text] [Related]
3. Haplotype analysis of congenital myotonic dystrophy patients from asymptomatic DM father.
Tachi N; Ohya K; Yamagata H; Miki T; Kikuchi K; Chiba S
Pediatr Neurol; 1997 May; 16(4):315-8. PubMed ID: 9258965
[TBL] [Abstract][Full Text] [Related]
4. Paternal transmission of congenital myotonic dystrophy.
de Die-Smulders CE; Smeets HJ; Loots W; Anten HB; Mirandolle JF; Geraedts JP; Höweler CJ
J Med Genet; 1997 Nov; 34(11):930-3. PubMed ID: 9391889
[TBL] [Abstract][Full Text] [Related]
5. Paternal transmission of the congenital form of myotonic dystrophy type 1: a new case and review of the literature.
Zeesman S; Carson N; Whelan DT
Am J Med Genet; 2002 Jan; 107(3):222-6. PubMed ID: 11807903
[TBL] [Abstract][Full Text] [Related]
6. Paternal transmission of congenital myotonic dystrophy.
Bergoffen J; Kant J; Sladky J; McDonald-McGinn D; Zackai EH; Fischbeck KH
J Med Genet; 1994 Jul; 31(7):518-20. PubMed ID: 7966187
[TBL] [Abstract][Full Text] [Related]
7. An intergenerational contraction of the CTG repeat in Japanese myotonic dystrophy.
Matsumura R; Namikawa T; Miki T; Kihira T; Yamagata H; Mano Y; Takayanagi T
J Neurol Sci; 1996 Jul; 139(1):48-51. PubMed ID: 8836971
[TBL] [Abstract][Full Text] [Related]
8. A case of paternally inherited congenital myotonic dystrophy.
Nakagawa M; Yamada H; Higuchi I; Kaminishi Y; Miki T; Johnson K; Osame M
J Med Genet; 1994 May; 31(5):397-400. PubMed ID: 8064819
[TBL] [Abstract][Full Text] [Related]
9. Effects of the sex of myotonic dystrophy patients on the unstable triplet repeat in their affected offspring.
Ashizawa T; Dunne PW; Ward PA; Seltzer WK; Richards CS
Neurology; 1994 Jan; 44(1):120-2. PubMed ID: 8290046
[TBL] [Abstract][Full Text] [Related]
10. Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy.
Tsilfidis C; MacKenzie AE; Mettler G; Barceló J; Korneluk RG
Nat Genet; 1992 Jun; 1(3):192-5. PubMed ID: 1303233
[TBL] [Abstract][Full Text] [Related]
11. Congenital myotonic dystrophy: report of paternal transmission.
Tanaka Y; Suzuki Y; Shimozawa N; Nanba E; Kondo N
Brain Dev; 2000 Mar; 22(2):132-4. PubMed ID: 10722967
[TBL] [Abstract][Full Text] [Related]
12. Molecular analysis of two pre-mutations in myotonic dystrophy.
Yamagata H; Kinoshita M; Komori T; Kondo I; Miki T
Clin Genet; 1998 Oct; 54(4):354-7. PubMed ID: 9831350
[TBL] [Abstract][Full Text] [Related]
13. CTG repeat size and histologic findings of skeletal muscle from patients with congenital myotonic dystrophy.
Tachi N; Kozuka N; Ohya K; Chiba S; Kikuchi K
J Child Neurol; 1996 Nov; 11(6):430-2. PubMed ID: 9120218
[TBL] [Abstract][Full Text] [Related]
14. Frequency of intergenerational contractions of the CTG repeats in myotonic dystrophy.
López de Munain A; Cobo AM; Sáenz A; Blanco A; Poza JJ; Martorell L; Martí-Massó JF; Baiget M
Genet Epidemiol; 1996; 13(5):483-7. PubMed ID: 8905394
[TBL] [Abstract][Full Text] [Related]
15. Anticipation in myotonic dystrophy type 1 parents with small CTG expansions.
Pratte A; Prévost C; Puymirat J; Mathieu J
Am J Med Genet A; 2015 Apr; 167A(4):708-14. PubMed ID: 25712547
[TBL] [Abstract][Full Text] [Related]
16. [A pedigree with myotonic dystrophy: non-CTG, non-CCTG repeat expansion].
Zhao XP; Xie HJ; Zheng HM; Yu ZL; Cui Y; Ding SJ; Ren DM; Tang GM
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Oct; 21(5):459-62. PubMed ID: 15476170
[TBL] [Abstract][Full Text] [Related]
17. [Advances in molecular genetics of myotonic dystrophy].
Yamagata H; Yamanaka N; Miki T; Ogihara T
Nihon Rinsho; 1993 Sep; 51(9):2474-80. PubMed ID: 8411731
[TBL] [Abstract][Full Text] [Related]
18. Contribution of molecular analyses to the estimation of the risk of congenital myotonic dystrophy.
Cobo AM; Poza JJ; Martorell L; López de Munain A; Emparanza JI; Baiget M
J Med Genet; 1995 Feb; 32(2):105-8. PubMed ID: 7760317
[TBL] [Abstract][Full Text] [Related]
19. [DNA analysis of a pedigree with myotonic dystrophy in Songjiang county, Shanghai].
Xie H; Zheng H; Zheng S; Deng B; Xu J; Cui Y; Wang Y; Xu Z; Ren D
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2000 Oct; 17(5):319-22. PubMed ID: 11024209
[TBL] [Abstract][Full Text] [Related]
20. Myotonic dystrophy: absence of CTG enlarged transcript in congenital forms, and low expression of the normal allele.
Hofmann-Radvanyi H; Lavedan C; Rabès JP; Savoy D; Duros C; Johnson K; Junien C
Hum Mol Genet; 1993 Aug; 2(8):1263-6. PubMed ID: 7691346
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]