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Genomic rearrangements in MSH2 and MLH1 are rare mutational events in Spanish patients with hereditary nonpolyposis colorectal cancer.
Castellví-Bel S, Castells A, Strunk M, Ferrández A, Piazuelo E, Milà M, Piñol V, Rodríguez-Moranta F, Andreu M, Lanas A, Piqué JM; Gastrointestinal Oncology Group of the Spanish Gastroenterological Association. Castellví-Bel S, et al. Among authors: mila m. Cancer Lett. 2005 Jul 8;225(1):93-8. doi: 10.1016/j.canlet.2005.01.036. Cancer Lett. 2005. PMID: 16003840
Novel MLH1 duplication identified in Colombian families with Lynch syndrome.
Alonso-Espinaco V, Giráldez MD, Trujillo C, van der Klift H, Muñoz J, Balaguer F, Ocaña T, Madrigal I, Jones AM, Echeverry MM, Velez A, Tomlinson I, Milà M, Wijnen J, Carvajal-Carmona L, Castells A, Castellví-Bel S. Alonso-Espinaco V, et al. Among authors: mila m. Genet Med. 2011 Feb;13(2):155-60. doi: 10.1097/GIM.0b013e318202e10b. Genet Med. 2011. PMID: 21233718 Free article.
Genes responsible for nonspecific mental retardation.
Castellví-Bel S, Milà M. Castellví-Bel S, et al. Among authors: mila m. Mol Genet Metab. 2001 Feb;72(2):104-8. doi: 10.1006/mgme.2000.3128. Mol Genet Metab. 2001. PMID: 11161835 Review.
High incidence of large deletions in the PMS2 gene in Spanish Lynch syndrome families.
Brea-Fernández AJ, Cameselle-Teijeiro JM, Alenda C, Fernández-Rozadilla C, Cubiella J, Clofent J, Reñé JM, Anido U, Milá M, Balaguer F, Castells A, Castellvi-Bel S, Jover R, Carracedo A, Ruiz-Ponte C. Brea-Fernández AJ, et al. Among authors: mila m. Clin Genet. 2014 Jun;85(6):583-8. doi: 10.1111/cge.12232. Epub 2013 Jul 28. Clin Genet. 2014. PMID: 23837913
Maternal transmission in sporadic Huntington's disease.
Sánchez A, Milà M, Castellví-Bel S, Rosich M, Jiménez D, Badenas C, Estivill X. Sánchez A, et al. Among authors: mila m. J Neurol Neurosurg Psychiatry. 1997 May;62(5):535-7. doi: 10.1136/jnnp.62.5.535. J Neurol Neurosurg Psychiatry. 1997. PMID: 9153618 Free PMC article.
189 results