Velasco E - Search Results

1

Dinucleotide repeat polymorphisms at the D5S1356, D5S1357 and D7S1480 loci.

Velasco E, de la Puente A, Cruces J, Valero MC, García-Patiño E, del Castillo I, Coloma A, Moreno F, Hernández-Chico C. Velasco E, et al. Hum Mol Genet. 1994 Aug;3(8):1441. doi: 10.1093/hmg/3.8.1441. Hum Mol Genet. 1994. PMID: 7987335 No abstract available.

2

Dinucleotide repeat polymorphism between the human C4BPA and C4BPB gene loci (1q32).

Velasco E, Sanchez-Corral P, Moreno F, Rodriguez de Cordoba S. Velasco E, et al. Hum Mol Genet. 1992 Oct;1(7):552. doi: 10.1093/hmg/1.7.552-a. Hum Mol Genet. 1992. PMID: 1307261 No abstract available.

3

Isolation of microsatellites from the spinal muscular atrophy (SMA) candidate region on chromosome 5q and linkage analysis in Spanish SMA families.

Velasco E, Valero C, García E, de la Puente A, Cruces J, San Millán JL, del Castillo I, Coloma A, Moreno F, Hernández-Chico C. Velasco E, et al. Eur J Hum Genet. 1995;3(2):96-101. doi: 10.1159/000472282. Eur J Hum Genet. 1995. PMID: 7552147

4

Dinucleotide repeat polymorphism at the D4S2458 locus close to the PKD2 locus on human chromosome 4q.

Viribay M, Tellería D, Velasco E, Moreno F, San Millán JL. Viribay M, et al. Among authors: velasco e. Hum Genet. 1995 May;95(5):601-2. doi: 10.1007/BF00223883. Hum Genet. 1995. PMID: 7759091

5

Characterization of four mutations in the neurofibromatosis type 1 gene by denaturing gradient gel electrophoresis (DGGE).

Valero MC, Velasco E, Moreno F, Hernández-Chico C. Valero MC, et al. Among authors: velasco e. Hum Mol Genet. 1994 Apr;3(4):639-41. doi: 10.1093/hmg/3.4.639. Hum Mol Genet. 1994. PMID: 8069310

6

Linkage disequilibrium between four intragenic polymorphic microsatellites of the NF1 gene and its implications for genetic counselling.

Valero MC, Velasco E, Valero A, Moreno F, Hernández-Chico C. Valero MC, et al. Among authors: velasco e. J Med Genet. 1996 Jul;33(7):590-3. doi: 10.1136/jmg.33.7.590. J Med Genet. 1996. PMID: 8818946 Free PMC article.

7

Molecular analysis of the SMN and NAIP genes in Spanish spinal muscular atrophy (SMA) families and correlation between number of copies of cBCD541 and SMA phenotype.

Velasco E, Valero C, Valero A, Moreno F, Hernández-Chico C. Velasco E, et al. Hum Mol Genet. 1996 Feb;5(2):257-63. doi: 10.1093/hmg/5.2.257. Hum Mol Genet. 1996. PMID: 8824882 Free article.

8

Identification of de novo deletions at the NF1 gene: no preferential paternal origin and phenotypic analysis of patients.

Valero MC, Pascual-Castroviejo I, Velasco E, Moreno F, Hernández-Chico C. Valero MC, et al. Among authors: velasco e. Hum Genet. 1997 Jun;99(6):720-6. doi: 10.1007/s004390050438. Hum Genet. 1997. PMID: 9187663

9

Analysis of the monomeric alphoid sequences in the pericentromeric region of human chromosome 7.

de la Puente A, Velasco E, Pérez Jurado LA, Hernández-Chico C, van de Rijke FM, Scherer SW, Raap AK, Cruces J. de la Puente A, et al. Among authors: velasco e. Cytogenet Cell Genet. 1998;83(3-4):176-81. doi: 10.1159/000015175. Cytogenet Cell Genet. 1998. PMID: 10072574

10

High proportion of novel mutations of BRCA1 and BRCA2 in breast/ovarian cancer patients from Castilla-León (central Spain).

Infante M, Durán M, Esteban-Cardeñosa E, Miner C, Velasco E. Infante M, et al. Among authors: velasco e. J Hum Genet. 2006;51(7):611-7. doi: 10.1007/s10038-006-0404-7. Epub 2006 Jun 7. J Hum Genet. 2006. PMID: 16758124 Free article.

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