Millán JM - Search Results

1

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

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

The p.R1109X mutation in SH3TC2 gene is predominant in Spanish Gypsies with Charcot-Marie-Tooth disease type 4.

Claramunt R, Sevilla T, Lupo V, Cuesta A, Millán JM, Vílchez JJ, Palau F, Espinós C. Claramunt R, et al. Among authors: millan jm. Clin Genet. 2007 Apr;71(4):343-9. doi: 10.1111/j.1399-0004.2007.00774.x. Clin Genet. 2007. PMID: 17470135

4

Genetics of the Charcot-Marie-Tooth disease in the Spanish Gypsy population: the hereditary motor and sensory neuropathy-Russe in depth.

Sevilla T, Martínez-Rubio D, Márquez C, Paradas C, Colomer J, Jaijo T, Millán JM, Palau F, Espinós C. Sevilla T, et al. Among authors: millan jm. Clin Genet. 2013 Jun;83(6):565-70. doi: 10.1111/cge.12015. Epub 2012 Oct 10. Clin Genet. 2013. PMID: 22978647

5

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

6

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

7

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.

8

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

9

Genetics of Charcot-Marie-Tooth disease type 4A: mutations, inheritance, phenotypic variability, and founder effect.

Claramunt R, Pedrola L, Sevilla T, López de Munain A, Berciano J, Cuesta A, Sánchez-Navarro B, Millán JM, Saifi GM, Lupski JR, Vílchez JJ, Espinós C, Palau F. Claramunt R, et al. Among authors: millan jm. J Med Genet. 2005 Apr;42(4):358-65. doi: 10.1136/jmg.2004.022178. J Med Genet. 2005. PMID: 15805163 Free PMC article. No abstract available.

10

Spanish MYH7 founder mutation of Italian ancestry causing a large cluster of Laing myopathy patients.

Muelas N, Hackman P, Luque H, Suominen T, Espinós C, Garcés-Sánchez M, Sevilla T, Azorín I, Millán JM, Udd B, Vílchez JJ. Muelas N, et al. Among authors: millan jm. Clin Genet. 2012 May;81(5):491-4. doi: 10.1111/j.1399-0004.2011.01667.x. Epub 2011 Apr 11. Clin Genet. 2012. PMID: 21395566

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

224 results

Search Page

Filters