Lázaro C - Search Results

1

Association study of proposed candidate genes/regions in a population of Spanish asthmatics.

Soriano JB, de Cid R, Estivill X, Antó JM, Sunyer J, Otero D, Roca J, Rodríguez-Roisín R, Morell F, Rodrigo MJ, Ercilla G, Beaty TH, Lázaro C. Soriano JB, et al. Among authors: lazaro c. Eur J Epidemiol. 2000;16(8):745-50. doi: 10.1023/a:1026758319621. Eur J Epidemiol. 2000. PMID: 11142503

2

Mutation analysis of genetic diseases by asymmetric-PCR SSCP and ethidium bromide staining: application to neurofibromatosis and cystic fibrosis.

Lázaro C, Estivill X. Lázaro C, et al. Mol Cell Probes. 1992 Oct;6(5):357-9. doi: 10.1016/0890-8508(92)90027-u. Mol Cell Probes. 1992. PMID: 1282203

3

Prenatal diagnosis of sporadic neurofibromatosis 1.

Lazaro C, Ravella A, Casals T, Volpini V, Estivill X. Lazaro C, et al. Lancet. 1992 Jan 11;339(8785):119-20. doi: 10.1016/0140-6736(92)91024-3. Lancet. 1992. PMID: 1345836 No abstract available.

4

Cystic fibrosis in the Basque country: high frequency of mutation delta F508 in patients of Basque origin.

Casals T, Vázquez C, Lázaro C, Girbau E, Giménez FJ, Estivill X. Casals T, et al. Among authors: lazaro c. Am J Hum Genet. 1992 Feb;50(2):404-10. Am J Hum Genet. 1992. PMID: 1370875 Free PMC article.

5

Recurrence of a nonsense mutation in the NF1 gene causing classical neurofibromatosis type 1.

Estivill X, Lázaro C, Casals T, Ravella A. Estivill X, et al. Among authors: lazaro c. Hum Genet. 1991 Dec;88(2):185-8. doi: 10.1007/BF00206069. Hum Genet. 1991. PMID: 1757093

6

Mutation and linkage disequilibrium analysis in genetic counselling of Spanish cystic fibrosis families.

Casals T, Nunes V, Lázaro C, Giménez FJ, Girbau E, Volpini V, Estivill X. Casals T, et al. Among authors: lazaro c. J Med Genet. 1991 Nov;28(11):771-6. doi: 10.1136/jmg.28.11.771. J Med Genet. 1991. PMID: 1770534 Free PMC article.

7

Molecular characterization of the breakpoints of a 12-kb deletion in the NF1 gene in a family showing germ-line mosaicism.

Lázaro C, Gaona A, Lynch M, Kruyer H, Ravella A, Estivill X. Lázaro C, et al. Am J Hum Genet. 1995 Nov;57(5):1044-9. Am J Hum Genet. 1995. PMID: 7485153 Free PMC article.

8

Two further cases of mutation R1947X in the NF1 gene: screening for a relatively common recurrent mutation.

Lázaro C, Kruyer H, Gaona A, Estivill X. Lázaro C, et al. Hum Genet. 1995 Sep;96(3):361-3. doi: 10.1007/BF00210425. Hum Genet. 1995. PMID: 7649559

9

Chromosome 9p deletions in cutaneous malignant melanoma tumors: the minimal deleted region involves markers outside the p16 (CDKN2) gene.

Puig S, Ruiz A, Lázaro C, Castel T, Lynch M, Palou J, Vilalta A, Weissenbach J, Mascaro JM, Estivill X. Puig S, et al. Among authors: lazaro c. Am J Hum Genet. 1995 Aug;57(2):395-402. Am J Hum Genet. 1995. PMID: 7668266 Free PMC article.

10

Predominant occurrence of somatic mutations of the NF2 gene in meningiomas and schwannomas.

Mérel P, Hoang-Xuan K, Sanson M, Moreau-Aubry A, Bijlsma EK, Lazaro C, Moisan JP, Resche F, Nishisho I, Estivill X, et al. Mérel P, et al. Among authors: lazaro c. Genes Chromosomes Cancer. 1995 Jul;13(3):211-6. doi: 10.1002/gcc.2870130311. Genes Chromosomes Cancer. 1995. PMID: 7669741

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