Arjona D - Search Results

1

Adapting ACMG/AMP sequence variant classification guidelines for single-gene copy number variants.

Brandt T, Sack LM, Arjona D, Tan D, Mei H, Cui H, Gao H, Bean LJH, Ankala A, Del Gaudio D, Knight Johnson A, Vincent LM, Reavey C, Lai A, Richard G, Meck JM. Brandt T, et al. Among authors: arjona d. Genet Med. 2020 Feb;22(2):336-344. doi: 10.1038/s41436-019-0655-2. Epub 2019 Sep 19. Genet Med. 2020. PMID: 31534211 Free article.

2

Correction: Adapting ACMG/AMP sequence variant classification guidelines for single-gene copy-number variants.

Brandt T, Sack LM, Arjona D, Tan D, Mei H, Cui H, Gao H, Bean LJH, Ankala A, Del Gaudio D, Johnson AK, Vincent LM, Reavey C, Lai A, Richard G, Meck JM. Brandt T, et al. Among authors: arjona d. Genet Med. 2020 Mar;22(3):670-671. doi: 10.1038/s41436-019-0725-5. Genet Med. 2020. PMID: 31844178 Free article.

3

Comment on the criteria for interpretation of mitochondrial tRNA variants.

Bai R, Balog A, Kiesler P, Arjona D, Cui H. Bai R, et al. Among authors: arjona d. Genet Med. 2020 Aug;22(8):1418-1419. doi: 10.1038/s41436-020-0804-7. Epub 2020 May 18. Genet Med. 2020. PMID: 32418987 Free article. No abstract available.

4

MLPA vs multiprobe FISH: comparison of two methods for the screening of subtelomeric rearrangements in 50 patients with idiopathic mental retardation.

Palomares M, Delicado A, Lapunzina P, Arjona D, Amiñoso C, Arcas J, Martinez Bermejo A, Fernández L, López Pajares I. Palomares M, et al. Among authors: arjona d. Clin Genet. 2006 Mar;69(3):228-33. doi: 10.1111/j.1399-0004.2006.00567.x. Clin Genet. 2006. PMID: 16542387

5

Comparative study of three diagnostic approaches (FISH, STRs and MLPA) in 30 patients with 22q11.2 deletion syndrome.

Fernández L, Lapunzina P, Arjona D, López Pajares I, García-Guereta L, Elorza D, Burgueros M, De Torres ML, Mori MA, Palomares M, García-Alix A, Delicado A. Fernández L, et al. Among authors: arjona d. Clin Genet. 2005 Oct;68(4):373-8. doi: 10.1111/j.1399-0004.2005.00493.x. Clin Genet. 2005. PMID: 16143025

6

CpG island methylation of tumor-related genes in three primary central nervous system lymphomas in immunocompetent patients.

Gonzalez-Gomez P, Bello MJ, Arjona D, Alonso ME, Lomas J, Amiñoso C, de Campos JM, Sarasa JL, Gutierrez M, Rey JA. Gonzalez-Gomez P, et al. Among authors: arjona d. Cancer Genet Cytogenet. 2003 Apr 1;142(1):21-4. doi: 10.1016/s0165-4608(02)00799-9. Cancer Genet Cytogenet. 2003. PMID: 12660028

7

Methylation status of TP73 in meningiomas.

Lomas J, Amiñoso C, Gonzalez-Gomez P, Eva Alonso M, Arjona D, Lopez-Marin I, de Campos JM, Isla A, Vaquero J, Gutierrez M, Sarasa JL, Josefa Bello M, Rey JA. Lomas J, et al. Among authors: arjona d. Cancer Genet Cytogenet. 2004 Jan 15;148(2):148-51. doi: 10.1016/s0165-4608(03)00244-9. Cancer Genet Cytogenet. 2004. PMID: 14734228

8

Genetic and epigenetic alteration of the NF2 gene in sporadic meningiomas.

Lomas J, Bello MJ, Arjona D, Alonso ME, Martinez-Glez V, Lopez-Marin I, Amiñoso C, de Campos JM, Isla A, Vaquero J, Rey JA. Lomas J, et al. Among authors: arjona d. Genes Chromosomes Cancer. 2005 Mar;42(3):314-9. doi: 10.1002/gcc.20141. Genes Chromosomes Cancer. 2005. PMID: 15609345

9

Aberrant methylation of multiple genes in neuroblastic tumours. relationship with MYCN amplification and allelic status at 1p.

Gonzalez-Gomez P, Bello MJ, Lomas J, Arjona D, Alonso ME, Amiñoso C, Lopez-Marin I, Anselmo NP, Sarasa JL, Gutierrez M, Casartelli C, Rey JA. Gonzalez-Gomez P, et al. Among authors: arjona d. Eur J Cancer. 2003 Jul;39(10):1478-85. doi: 10.1016/s0959-8049(03)00312-5. Eur J Cancer. 2003. PMID: 12826052

10

Molecular analysis of the EGFR gene in astrocytic gliomas: mRNA expression, quantitative-PCR analysis of non-homogeneous gene amplification and DNA sequence alterations.

Arjona D, Bello MJ, Alonso ME, Aminoso C, Isla A, De Campos JM, Sarasa JL, Gutierrez M, Villalobo A, Rey JA. Arjona D, et al. Neuropathol Appl Neurobiol. 2005 Aug;31(4):384-94. doi: 10.1111/j.1365-2990.2005.00653.x. Neuropathol Appl Neurobiol. 2005. PMID: 16008822

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