Johnson K - Search Results

1

Comparison of CTG repeat length expansion and clinical progression of myotonic dystrophy over a five year period.

Martorell L, Martinez JM, Carey N, Johnson K, Baiget M. Martorell L, et al. Among authors: johnson k. J Med Genet. 1995 Aug;32(8):593-6. doi: 10.1136/jmg.32.8.593. J Med Genet. 1995. PMID: 7473648 Free PMC article.

2

Progression of somatic CTG repeat length heterogeneity in the blood cells of myotonic dystrophy patients.

Martorell L, Monckton DG, Gamez J, Johnson KJ, Gich I, Lopez de Munain A, Baiget M. Martorell L, et al. Among authors: johnson kj. Hum Mol Genet. 1998 Feb;7(2):307-12. doi: 10.1093/hmg/7.2.307. Hum Mol Genet. 1998. PMID: 9425239

3

Expansion of the myotonic dystrophy gene in Italian and Spanish patients.

Melchionda S, Cobo A, Gennarelli M, Martorell L, Fattorini C, Baiget M, Lopez de Munain A, Johnson K, Shelbourne P, Novelli G, et al. Melchionda S, et al. Among authors: johnson k. J Med Genet. 1992 Nov;29(11):789-90. doi: 10.1136/jmg.29.11.789. J Med Genet. 1992. PMID: 1453428 Free PMC article.

4

Direct molecular analysis of myotonic dystrophy in the German population: important considerations in genetic counselling.

Meiner A, Wolf C, Carey N, Okitsu A, Johnson K, Shelbourne P, Kunath B, Sauermann W, Thiele H, Kupferling P, et al. Meiner A, et al. Among authors: johnson k. J Med Genet. 1995 Aug;32(8):645-9. doi: 10.1136/jmg.32.8.645. J Med Genet. 1995. PMID: 7473660 Free PMC article.

5

[Direct genotypic analysis of myotonic dystrophy: detection of an unstable DNA fragment in carriers].

Cobo AM, Martorell L, López de Munain A, Basauri B, Martínez JM, Johnson K, Baiget M. Cobo AM, et al. Among authors: johnson k. Med Clin (Barc). 1993 Mar 13;100(10):361-4. Med Clin (Barc). 1993. PMID: 8097270 Spanish.

6

Molecular diagnosis of homozygous myotonic dystrophy in two asymptomatic sisters.

Cobo A, Martinez JM, Martorell L, Baiget M, Johnson K. Cobo A, et al. Among authors: johnson k. Hum Mol Genet. 1993 Jun;2(6):711-5. doi: 10.1093/hmg/2.6.711. Hum Mol Genet. 1993. PMID: 8353490

7

Somatic instability of the myotonic dystrophy (CTG)n repeat during human fetal development.

Martorell L, Johnson K, Boucher CA, Baiget M. Martorell L, et al. Among authors: johnson k. Hum Mol Genet. 1997 Jun;6(6):877-80. doi: 10.1093/hmg/6.6.877. Hum Mol Genet. 1997. PMID: 9175733

8

Is myotonic dystrophy a single-gene disorder?

Johnson KJ, Boucher Ca, King SK, Winchester CL, Bailey ME, Hamilton GM, Carey N. Johnson KJ, et al. Biochem Soc Trans. 1996 May;24(2):510-3. doi: 10.1042/bst0240510. Biochem Soc Trans. 1996. PMID: 8736794 Review. No abstract available.

9

Meiotic drive at the myotonic dystrophy locus?

Carey N, Johnson K, Nokelainen P, Peltonen L, Savontaus ML, Juvonen V, Anvret M, Grandell U, Chotai K, Robertson E, et al. Carey N, et al. Among authors: johnson k. Nat Genet. 1994 Feb;6(2):117-8. doi: 10.1038/ng0294-117. Nat Genet. 1994. PMID: 8162064 No abstract available.

10

Sex-related difference in intergenerational expansion of myotonic dystrophy gene.

Cobo AM, Baiget M, López de Munain A, Poza JJ, Emparanza JI, Johnson K. Cobo AM, et al. Among authors: johnson k. Lancet. 1993 May 1;341(8853):1159-60. doi: 10.1016/0140-6736(93)93186-5. Lancet. 1993. PMID: 8097850 No abstract available.

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