Robledo M - Search Results

1

G12S and H50R variations are polymorphisms in the SDHD gene.

Cascón A, Ruiz-Llorente S, Cebrián A, Letón R, Tellería D, Benítez J, Robledo M. Cascón A, et al. Among authors: robledo m. Genes Chromosomes Cancer. 2003 Jun;37(2):220-1. doi: 10.1002/gcc.10212. Genes Chromosomes Cancer. 2003. PMID: 12696072 No abstract available.

2

Molecular analysis of the BRCA2 gene in 16 breast/ovarian cancer Spanish families.

Osorio A, Robledo M, Martínez B, Cebrián A, San Román JM, Albertos J, Lobo F, Benítez J. Osorio A, et al. Among authors: robledo m. Clin Genet. 1998 Aug;54(2):142-7. doi: 10.1111/j.1399-0004.1998.tb03717.x. Clin Genet. 1998. PMID: 9761393

3

[Identification of a de novo mutation in a patient without von Hippel-Lindau syndrome: clinical and diagnostic implications].

Cebrián A, Ruiz Barnés P, Osorio A, Martínez-Delgado B, Benítez J, Robledo M. Cebrián A, et al. Among authors: robledo m. Neurologia. 1999 Aug-Sep;14(7):362-5. Neurologia. 1999. PMID: 10570625 Spanish.

4

Identification by comparative genomic hybridization of genetic changes involved in tumoral progression of a T-cell non-Hodgkin lymphoma.

Arranz E, Martínez-Delgado B, Richart A, Osorio A, Cebrián A, Robledo M, Rivas C, Benítez J. Arranz E, et al. Among authors: robledo m. Cancer Genet Cytogenet. 2000 Feb;117(1):41-4. doi: 10.1016/s0165-4608(99)00139-9. Cancer Genet Cytogenet. 2000. PMID: 10700865

5

Molecular analysis of the BRCA1 and BRCA2 genes in 32 breast and/or ovarian cancer Spanish families.

Osorio A, Barroso A, Martínez B, Cebrián A, San Román JM, Lobo F, Robledo M, Benítez J. Osorio A, et al. Among authors: robledo m. Br J Cancer. 2000 Apr;82(7):1266-70. doi: 10.1054/bjoc.1999.1089. Br J Cancer. 2000. PMID: 10755399 Free PMC article.

6

Hypermethylation of P16ink4a and P15ink4b genes as a marker of disease in the follow-up of non-Hodgkin's lymphomas.

Martinez-Delgado B, Richart A, García MJ, Robledo M, Osorio A, Cebrian A, Rivas C, Benitez J. Martinez-Delgado B, et al. Among authors: robledo m. Br J Haematol. 2000 Apr;109(1):97-103. doi: 10.1046/j.1365-2141.2000.01991.x. Br J Haematol. 2000. PMID: 10848787 Free article.

7

Identification of novel SDHD mutations in patients with phaeochromocytoma and/or paraganglioma.

Cascon A, Ruiz-Llorente S, Cebrian A, Telleria D, Rivero JC, Diez JJ, Lopez-Ibarra PJ, Jaunsolo MA, Benitez J, Robledo M. Cascon A, et al. Among authors: robledo m. Eur J Hum Genet. 2002 Aug;10(8):457-61. doi: 10.1038/sj.ejhg.5200829. Eur J Hum Genet. 2002. PMID: 12111639

8

A rapid and easy method for multiple endocrine neoplasia type 1 mutation detection using conformation-sensitive gel electrophoresis.

Arancha C, Ruíz-Llorente S, Cascón A, Osorio A, Martínez-Delgado B, Benítez J, Robledo M. Arancha C, et al. Among authors: robledo m. J Hum Genet. 2002;47(4):190-5. doi: 10.1007/s100380200022. J Hum Genet. 2002. PMID: 12166655

9

SDHB mutation analysis in familial and sporadic phaeochromocytoma identifies a novel mutation.

Cascón A, Cebrián A, Ruiz-Llorente S, Tellería D, Benítez J, Robledo M. Cascón A, et al. Among authors: robledo m. J Med Genet. 2002 Oct;39(10):E64. doi: 10.1136/jmg.39.10.e64. J Med Genet. 2002. PMID: 12362046 Free PMC article. No abstract available.

10

Molecular study of a new family with hereditary renal cell carcinoma and a translocation t(3;8)(p13;q24.1).

Meléndez B, Rodríguez-Perales S, Martínez-Delgado B, Otero I, Robledo M, Martínez-Ramírez A, Ruiz-Llorente S, Urioste M, Cigudosa JC, Benítez J. Meléndez B, et al. Among authors: robledo m. Hum Genet. 2003 Feb;112(2):178-85. doi: 10.1007/s00439-002-0848-6. Epub 2002 Nov 13. Hum Genet. 2003. PMID: 12522559

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