Baiget M - Search Results

1

Homozygous myotonic dystrophy: clinical and molecular studies of three unrelated cases.

Martorell L, Illa I, Rosell J, Benitez J, Sedano MJ, Baiget M. Martorell L, et al. Among authors: baiget m. J Med Genet. 1996 Sep;33(9):783-5. doi: 10.1136/jmg.33.9.783. J Med Genet. 1996. PMID: 8880582 Free PMC article.

2

Complex patterns of male germline instability and somatic mosaicism in myotonic dystrophy type 1.

Martorell L, Monckton DG, Gamez J, Baiget M. Martorell L, et al. Among authors: baiget m. Eur J Hum Genet. 2000 Jun;8(6):423-30. doi: 10.1038/sj.ejhg.5200478. Eur J Hum Genet. 2000. PMID: 10878662 Free article.

3

Frequency and stability of the myotonic dystrophy type 1 premutation.

Martorell L, Monckton DG, Sanchez A, Lopez De Munain A, Baiget M. Martorell L, et al. Among authors: baiget m. Neurology. 2001 Feb 13;56(3):328-35. doi: 10.1212/wnl.56.3.328. Neurology. 2001. PMID: 11171897

4

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: baiget m. 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.

5

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. Cobo AM, et al. Among authors: baiget m. J Med Genet. 1995 Feb;32(2):105-8. doi: 10.1136/jmg.32.2.105. J Med Genet. 1995. PMID: 7760317 Free PMC article.

6

[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: baiget m. Med Clin (Barc). 1993 Mar 13;100(10):361-4. Med Clin (Barc). 1993. PMID: 8097270 Spanish.

7

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: baiget m. Hum Mol Genet. 1993 Jun;2(6):711-5. doi: 10.1093/hmg/2.6.711. Hum Mol Genet. 1993. PMID: 8353490

8

Influence of the sex of the transmitting grandparent in congenital myotonic dystrophy.

López de Munain A, Cobo AM, Poza JJ, Navarrete D, Martorell L, Palau F, Emparanza JI, Baiget M. López de Munain A, et al. Among authors: baiget m. J Med Genet. 1995 Sep;32(9):689-91. doi: 10.1136/jmg.32.9.689. J Med Genet. 1995. PMID: 8544186 Free PMC article.

9

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: baiget m. Hum Mol Genet. 1997 Jun;6(6):877-80. doi: 10.1093/hmg/6.6.877. Hum Mol Genet. 1997. PMID: 9175733

10

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: baiget m. Hum Mol Genet. 1998 Feb;7(2):307-12. doi: 10.1093/hmg/7.2.307. Hum Mol Genet. 1998. PMID: 9425239

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