Millán JM - 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: millan jm. Am J Med Genet. 2001 Aug 1;102(2):200-4. doi: 10.1002/ajmg.1416. Am J Med Genet. 2001. PMID: 11477616

2

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. Hum Genet. 1995 Aug;96(2):216-8. doi: 10.1007/BF00207382. Hum Genet. 1995. PMID: 7635473

3

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. Among authors: millan jm. 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.

4

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: millan jm. Cancer Genet Cytogenet. 1998 Apr 15;102(2):93-9. doi: 10.1016/s0165-4608(97)00343-9. Cancer Genet Cytogenet. 1998. PMID: 9546059

5

Mutation of the XNP/ATR-X gene in a family with severe mental retardation, spastic paraplegia and skewed pattern of X inactivation: demonstration that the mutation is involved in the inactivation bias.

Lossi AM, Millán JM, Villard L, Orellana C, Cardoso C, Prieto F, Fontés M, Martínez F. Lossi AM, et al. Among authors: millan jm. Am J Hum Genet. 1999 Aug;65(2):558-62. doi: 10.1086/302499. Am J Hum Genet. 1999. PMID: 10417298 Free PMC article. No abstract available.

6

Trisomy rescue by postzygotic unbalanced (X;14) translocation in a girl with dysmorphic features.

Orellana C, Martínez F, Badía L, Millán JM, Montero MR, Andrés J, Prieto F. Orellana C, et al. Among authors: millan jm. Clin Genet. 2001 Sep;60(3):206-11. doi: 10.1034/j.1399-0004.2001.600306.x. Clin Genet. 2001. PMID: 11595022

7

Clinical and genetic aspects of two Spanish families with autosomal dominant retinitis pigmentosa (ADRP).

Vilela C, Beneyto M, Bosch R, Millan JM, Marco M, Vallet M, Alonso L, Tormos I, Najera C, Valls B, Paricio N, Prieto F. Vilela C, et al. Among authors: millan jm. Ophthalmic Genet. 1996 Mar;17(1):29-33. doi: 10.3109/13816819609057866. Ophthalmic Genet. 1996. PMID: 8740695

8

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: millan jm. Hum Genet. 1997 Jun;99(6):746-54. doi: 10.1007/s004390050442. Hum Genet. 1997. PMID: 9187667

9

Epidemiology of retinitis pigmentosa in the Valencian community (Spain).

Nájera C, Millán JM, Beneyto M, Prieto F. Nájera C, et al. Among authors: millan jm. Genet Epidemiol. 1995;12(1):37-46. doi: 10.1002/gepi.1370120105. Genet Epidemiol. 1995. PMID: 7713399 Review.

10

X-linked anhidrotic (hypohidrotic) ectodermal dysplasia caused by a novel mutation in EDA1 gene: 406T > G (Leu55Arg).

Martínez F, Millán JM, Orellana C, Prieto F. Martínez F, et al. Among authors: millan jm. J Invest Dermatol. 1999 Aug;113(2):285-6. doi: 10.1046/j.1523-1747.1999.00656.x. J Invest Dermatol. 1999. PMID: 10469321 Free article. No abstract available.

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