Baiget M - Search Results

1

[Use of dystrophin c-DNA for the direct diagnosis of Duchenne muscular dystrophy in female carriers].

Baiget M, del Río E, Gallano P. Baiget M, et al. Neurologia. 1989 Oct;4(8):268-76. Neurologia. 1989. PMID: 2576910 Spanish.

2

[Dystrophinopathies].

Gallano P, Lasa A, Baiget M. Gallano P, et al. Among authors: baiget m. Neurologia. 1995 Dec;10 Suppl 1:8-11. Neurologia. 1995. PMID: 8838554 Review. Spanish.

3

[Molecular genetics in neurology (II). Analysis of the human genome].

Palau F, Baiget M, Gallano P. Palau F, et al. Among authors: baiget m. Neurologia. 1991 Oct;6(8):302-6. Neurologia. 1991. PMID: 1790008 Review. Spanish. No abstract available.

4

[Molecular genetics in neurology (I). Diagnostic strategies in the genotypic study of monogenic hereditary pathology].

Baiget M, Gallano P, Palau F. Baiget M, et al. Neurologia. 1991 Aug-Sep;6(7):263-5. Neurologia. 1991. PMID: 1685088 Review. Spanish. No abstract available.

5

Three novel point mutations in the dystrophin gene in DMD patients.

Lasa A, Gallano P, Baiget M. Lasa A, et al. Among authors: baiget m. Hum Mutat. 1997;9(5):473-4. doi: 10.1002/(SICI)1098-1004(1997)9:5<473::AID-HUMU15>3.0.CO;2-#. Hum Mutat. 1997. PMID: 9143930 No abstract available.

6

DMD carrier detection in a female with mosaic Turner's syndrome.

Baiget M, Tizzano E, Volpini V, del Rio E, Pérez-Vidal T, Gallano P. Baiget M, et al. J Med Genet. 1991 Mar;28(3):209-10. doi: 10.1136/jmg.28.3.209. J Med Genet. 1991. PMID: 2051460 Free PMC article. No abstract available.

7

[Use of the recombinant DNA technic in studying cystic fibrosis in 14 Spanish families: detection of carriers and healthy subjects].

Fernández García E, Benítez Ortiz J, Villamar López M, Ayuso García C, Ramos Corrales C, Sánchez Cascos A, Baiget M, Del Río E. Fernández García E, et al. Among authors: baiget m. An Esp Pediatr. 1989 Apr;30(4):251-4. An Esp Pediatr. 1989. PMID: 2568107 Spanish.

8

A novel insertional mutation of a single base on exon 12 of the dystrophin gene.

Lasa A, Gallano P, Colomer J, Baiget M. Lasa A, et al. Among authors: baiget m. Clin Genet. 1995 Sep;48(3):128-30. doi: 10.1111/j.1399-0004.1995.tb04071.x. Clin Genet. 1995. PMID: 8556818

9

[Prenatal diagnosis in a family carrying the fragile X syndrome using recombinant DNA technics].

Benítez J, Fernández E, Ramos C, Nunes V, del Río E, Baiget M. Benítez J, et al. Among authors: baiget m. Rev Clin Esp. 1989 Apr;184(7):364-6. Rev Clin Esp. 1989. PMID: 2570446 Spanish.

10

[Alterations in functional proteins. Calpaine-3 deficiency].

López de Munain A, Urtasun A, Poza JJ, Ruiz J, Sáenz A, Cobo AM, Lasa A, Gallano P, Baiget M, Martí-Massó JF. López de Munain A, et al. Among authors: baiget m. Rev Neurol. 1999 Jan 16-31;28(2):158-64. Rev Neurol. 1999. PMID: 10101785 Review. Spanish.

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