Baiget M - Search Results

1

Linkage disequilibrium detected between myotonic dystrophy and the anonymous marker D19S63 in the Spanish population.

Cobo A, Grinberg D, Balcells S, Vilageliu L, Gonzàlez-Duarte R, Baiget M. Cobo A, et al. Among authors: baiget m. Hum Genet. 1992 May;89(3):287-91. doi: 10.1007/BF00220541. Hum Genet. 1992. PMID: 1351033

2

3' creatine kinase (M-type) polymorphisms linked to myotonic dystrophy in Italian and Spanish populations.

Gennarelli M, Novelli G, Cobo A, Baiget M, Dallapiccola B. Gennarelli M, et al. Among authors: baiget m. Hum Genet. 1991 Oct;87(6):654-6. doi: 10.1007/BF00201719. Hum Genet. 1991. PMID: 1682233

3

[Application of the polymerase chain reaction technique (PCR) to the molecular diagnosis of myotonic dystrophy].

Cobo AM, Martínez JM, López de Munain A, Baiget M. Cobo AM, et al. Among authors: baiget m. Neurologia. 1991 Nov;6(9):317-21. Neurologia. 1991. PMID: 1687310 Spanish.

4

[Genetic analysis of Spanish families with myotonic dystrophy].

Cobo AM, Martínez JM, Pradas J, Baiget M. Cobo AM, et al. Among authors: baiget m. Neurologia. 1990 Mar;5(3):86-91. Neurologia. 1990. PMID: 2361046 Spanish.

5

Evidence against involvement of recoverin in autosomal recessive retinitis pigmentosa in 42 Spanish families.

Bayés M, Valverde D, Balcells S, Grinberg D, Vilageliu L, Benítez J, Ayuso C, Beneyto M, Baiget M, Gonzàlez-Duarte R. Bayés M, et al. Among authors: baiget m. Hum Genet. 1995 Jul;96(1):89-94. doi: 10.1007/BF00214192. Hum Genet. 1995. PMID: 7607661

6

Genetic fine localization of the arrestin (S-antigen) gene 4 cM distal from D2S172.

Valverde D, Bayés M, Martínez I, Grinberg D, Vilageliu L, Balcells S, Gonzàlez-Duarte R, Baiget M. Valverde D, et al. Among authors: baiget m. Hum Genet. 1994 Aug;94(2):193-4. doi: 10.1007/BF00202869. Hum Genet. 1994. PMID: 8045567

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

A novel mutation in exon 17 of the beta-subunit of rod phosphodiesterase in two RP sisters of a consanguineous family.

Valverde D, Solans T, Grinberg D, Balcells S, Vilageliu L, Bayés M, Chivelet P, Besmond C, Goossens M, González-Duarte R, Baiget M. Valverde D, et al. Among authors: baiget m. Hum Genet. 1996 Jan;97(1):35-8. doi: 10.1007/BF00218829. Hum Genet. 1996. PMID: 8557257

9

Identification of a novel R552O mutation in exon 13 of the beta-subunit of rod phosphodiesterase gene in a Spanish family with autosomal recessive retinitis pigmentosa.

Valverde D, Baiget M, Seminago R, del Rio E, García-Sandoval B, del Rio T, Bayés M, Balcells S, Martínez A, Grinberg D, Ayuso C. Valverde D, et al. Among authors: baiget m. Hum Mutat. 1996;8(4):393-4. doi: 10.1002/humu.1380080403. Hum Mutat. 1996. PMID: 8956055 No abstract available.

10

Autosomal recessive retinitis pigmentosa in Spain: evaluation of four genes and two loci involved in the disease.

Bayés M, Martínez-Mir A, Valverde D, del Río E, Vilageliu L, Grinberg D, Balcells S, Ayuso C, Baiget M, Gonzàlez-Duarte R. Bayés M, et al. Among authors: baiget m. Clin Genet. 1996 Nov;50(5):380-7. doi: 10.1111/j.1399-0004.1996.tb02392.x. Clin Genet. 1996. PMID: 9007328 Free article.

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