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Page 1
Variability in Phelan-McDermid Syndrome in a Cohort of 210 Individuals.
Nevado J, García-Miñaúr S, Palomares-Bralo M, Vallespín E, Guillén-Navarro E, Rosell J, Bel-Fenellós C, Mori MÁ, Milá M, Del Campo M, Barrúz P, Santos-Simarro F, Obregón G, Orellana C, Pachajoa H, Tenorio JA, Galán E, Cigudosa JC, Moresco A, Saleme C, Castillo S, Gabau E, Pérez-Jurado L, Barcia A, Martín MS, Mansilla E, Vallcorba I, García-Murillo P, Cammarata-Scalisi F, Gonçalves Pereira N, Blanco-Lago R, Serrano M, Ortigoza-Escobar JD, Gener B, Seidel VA, Tirado P, Lapunzina P; Spanish PMS Working Group. Nevado J, et al. Among authors: vallcorba i. Front Genet. 2022 Apr 12;13:652454. doi: 10.3389/fgene.2022.652454. eCollection 2022. Front Genet. 2022. PMID: 35495150 Free PMC article.
Prenatal ultrasound findings in Koolen-de Vries foetuses: Central nervous system anomalies are frequent markers of this syndrome.
García-Santiago FA, Martínez-Payo C, Mansilla E, Santos-Simarro F, Ruiz de Azua Ballesteros M, Mori MÁ, Antolín Alvarado E, Nieto Y, Vallcorba I, Tenorio J, Nevado J, Lapunzina P. García-Santiago FA, et al. Among authors: vallcorba i. Mol Genet Genomic Med. 2021 May;9(5):e1649. doi: 10.1002/mgg3.1649. Epub 2021 Mar 18. Mol Genet Genomic Med. 2021. PMID: 33733630 Free PMC article.
Euchromatic variant 16p+. Implications in prenatal diagnosis.
López Pajares I, Villa O, Salido M, Mori MA, Gonzalez A, Lapunzina P, De Torres ML, Vallcorba I, Palomares M, Fernández L, Delicado A. López Pajares I, et al. Among authors: vallcorba i. Prenat Diagn. 2006 Jun;26(6):535-8. doi: 10.1002/pd.1454. Prenat Diagn. 2006. PMID: 16634122
Cytogenetic study of neuroendocrine carcinoma of Merkel cells.
Vázquez-Mazariego Y, Vallcorba I, Ferro MT, López-Yarto A, García-Sagredo JM, Cabello P, Resino M, Muñoz R, Mayayo M, San Román C. Vázquez-Mazariego Y, et al. Among authors: vallcorba i. Cancer Genet Cytogenet. 1996 Nov;92(1):79-81. doi: 10.1016/0165-4608(94)00189-8. Cancer Genet Cytogenet. 1996. PMID: 8956877
Application of FISH 7q in MDS patients without monosomy 7 or 7q deletion by conventional G-banding cytogenetics: does -7/7q- detection by FISH have prognostic value?
Ademà V, Hernández JM, Abáigar M, Lumbreras E, Such E, Calull A, Dominguez E, Arenillas L, Mallo M, Cervera J, Marugán I, Tormo M, García F, González T, Luño E, Sanzo C, Martín ML, Fernández M, Costa D, Blázquez B, Barreña B, Marco F, Batlle A, Buño I, Martínez-Laperche C, Noriega V, Collado R, Ivars D, Carbonell F, Vallcorba I, Melero J, Delgado E, Vargas MT, Grau J, Salido M, Espinet B, Melero C, Florensa L, Pedro C, Solé F. Ademà V, et al. Among authors: vallcorba i. Leuk Res. 2013 Apr;37(4):416-21. doi: 10.1016/j.leukres.2012.12.010. Epub 2013 Jan 18. Leuk Res. 2013. PMID: 23337401
Memory T Cells Expressing an NKG2D-CAR Efficiently Target Osteosarcoma Cells.
Fernández L, Metais JY, Escudero A, Vela M, Valentín J, Vallcorba I, Leivas A, Torres J, Valeri A, Patiño-García A, Martínez J, Leung W, Pérez-Martínez A. Fernández L, et al. Among authors: vallcorba i. Clin Cancer Res. 2017 Oct 1;23(19):5824-5835. doi: 10.1158/1078-0432.CCR-17-0075. Epub 2017 Jun 28. Clin Cancer Res. 2017. PMID: 28659311
Chromosome 21 tandem repetition and AML1 (RUNX1) gene amplification.
Ferro MT, Hernaez R, Sordo MT, Garcia-Sagredo JM, Garcia-Miguel P, Fernández Guijarro M, Lopez J, Villalón C, Vallcorba I, Cabello P, San Roman C. Ferro MT, et al. Among authors: vallcorba i. Cancer Genet Cytogenet. 2004 Feb;149(1):11-6. doi: 10.1016/s0165-4608(03)00259-0. Cancer Genet Cytogenet. 2004. PMID: 15104277
15 results