Martínez F - Search Results

1

Localization of non-specific X-linked mental retardation gene (MRX73) to Xp22.2.

Martínez F, Martínez-Garay I, Millán JM, Pérez-Aytes A, Moltó MD, Orellana C, Prieto F. Martínez F, et al. Among authors: martinez garay i. Am J Med Genet. 2001 Aug 1;102(2):200-4. doi: 10.1002/ajmg.1416. Am J Med Genet. 2001. PMID: 11477616

2

A fragile X family with high penetrance in females: risk heterogeneity?

Martínez F, Badía L, Prieto F. Martínez F, et al. Clin Genet. 1992 Jul;42(1):22-6. doi: 10.1111/j.1399-0004.1992.tb03130.x. Clin Genet. 1992. PMID: 1355415

3

An autosomal dominant retinitis pigmentosa family with close linkage to D7S480 on 7q.

Millán JM, Martínez F, Vilela C, Beneyto M, Prieto F, Nájera C. Millán JM, et al. Among authors: martinez f. Hum Genet. 1995 Aug;96(2):216-8. doi: 10.1007/BF00207382. Hum Genet. 1995. PMID: 7635473

4

Localization of a gene for X-linked nonspecific mental retardation (MRX24) in Xp22.2-p22.3.

Martínez F, Gal A, Palau F, Prieto F. Martínez F, et al. Am J Med Genet. 1995 Jan 30;55(3):387-90. doi: 10.1002/ajmg.1320550328. Am J Med Genet. 1995. PMID: 7726242

5

Refined localization of the Prieto-syndrome locus.

Martínez F, Prieto F, Gal A. Martínez F, et al. Am J Med Genet. 1996 Jul 12;64(1):82. doi: 10.1002/(SICI)1096-8628(19960712)64:1<82::AID-AJMG14>3.0.CO;2-O. Am J Med Genet. 1996. PMID: 8826455 No abstract available.

6

Evidence for a common origin of most Friedreich ataxia chromosomes in the Spanish population.

Monrós E, Cañizares J, Moltó MD, Rodius F, Montermini L, Cossée M, Martínez F, Prieto F, de Frutos R, Koenig M, Pandolfo M, Bertranpetit J, Palau F. Monrós E, et al. Among authors: martinez f. Eur J Hum Genet. 1996;4(4):191-8. doi: 10.1159/000472198. Eur J Hum Genet. 1996. PMID: 8875184

7

Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies.

Bort S, Nelis E, Timmerman V, Sevilla T, Cruz-Martínez A, Martínez F, Millán JM, Arpa J, Vílchez JJ, Prieto F, Van Broeckhoven C, Palau F. Bort S, et al. Among authors: martinez f. Hum Genet. 1997 Jun;99(6):746-54. doi: 10.1007/s004390050442. Hum Genet. 1997. PMID: 9187667

8

Phenotype correlation and intergenerational dynamics of the Friedreich ataxia GAA trinucleotide repeat.

Monrós E, Moltó MD, Martínez F, Cañizares J, Blanca J, Vílchez JJ, Prieto F, de Frutos R, Palau F. Monrós E, et al. Among authors: martinez f. Am J Hum Genet. 1997 Jul;61(1):101-10. doi: 10.1086/513887. Am J Hum Genet. 1997. PMID: 9245990 Free PMC article.

9

Pediatric brain tumors: loss of heterozygosity at 17p and TP53 gene mutations.

Orellana C, Hernandez-Martí M, Martínez F, Castel V, Millán JM, Alvarez-Garijo JA, Prieto F, Badía L. Orellana C, et al. Among authors: martinez f. Cancer Genet Cytogenet. 1998 Apr 15;102(2):93-9. doi: 10.1016/s0165-4608(97)00343-9. Cancer Genet Cytogenet. 1998. PMID: 9546059

10

Genetic localisation of mental retardation with spastic diplegia to the pericentromeric region of the X chromosome: X inactivation in female carriers.

Martínez F, Tomás M, Millán JM, Fernández A, Palau F, Prieto F. Martínez F, et al. J Med Genet. 1998 Apr;35(4):284-7. doi: 10.1136/jmg.35.4.284. J Med Genet. 1998. PMID: 9598720 Free PMC article.

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