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Page 1
Detection of common chromosomal translocations in small round blue cell pediatric tumors.
Ponce-Castañeda MV, García-Chéquer AJ, Eguía Aguilar P, Abundes-Ramírez MA, Hernández-Angeles A, Nieto-Martínez K, Gómez-Laguna L, Sadowinski-Pine S, Cabrera-Muñoz Mde L. Ponce-Castañeda MV, et al. Among authors: gomez laguna l. Arch Med Res. 2014 Feb;45(2):143-51. doi: 10.1016/j.arcmed.2013.12.009. Epub 2014 Jan 28. Arch Med Res. 2014. PMID: 24486246
Amplified genes may be overexpressed, unchanged, or downregulated in cervical cancer cell lines.
Vazquez-Mena O, Medina-Martinez I, Juárez-Torres E, Barrón V, Espinosa A, Villegas-Sepulveda N, Gómez-Laguna L, Nieto-Martínez K, Orozco L, Roman-Basaure E, Muñoz Cortez S, Borges Ibañez M, Venegas-Vega C, Guardado-Estrada M, Rangel-López A, Kofman S, Berumen J. Vazquez-Mena O, et al. Among authors: gomez laguna l. PLoS One. 2012;7(3):e32667. doi: 10.1371/journal.pone.0032667. Epub 2012 Mar 7. PLoS One. 2012. PMID: 22412903 Free PMC article.
Diagnosis of familial Wolf-Hirschhorn syndrome due to a paternal cryptic chromosomal rearrangement by conventional and molecular cytogenetic techniques.
Venegas-Vega CA, Fernández-Ramírez F, Zepeda LM, Nieto-Martínez K, Gómez-Laguna L, Garduño-Zarazúa LM, Berumen J, Kofman S, Cervantes A. Venegas-Vega CA, et al. Among authors: gomez laguna l. Biomed Res Int. 2013;2013:209204. doi: 10.1155/2013/209204. Epub 2013 Feb 3. Biomed Res Int. 2013. PMID: 23484094 Free PMC article.
Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes.
Cervantes A, García-Delgado C, Fernández-Ramírez F, Galaz-Montoya C, Morales-Jiménez AB, Nieto-Martínez K, Gómez-Laguna L, Villa-Morales J, Quintana-Palma M, Berúmen J, Kofman S, Morán-Barroso VF. Cervantes A, et al. Among authors: gomez laguna l. BMC Med Genomics. 2014 Sep 15;7:55. doi: 10.1186/1755-8794-7-55. BMC Med Genomics. 2014. PMID: 25223409 Free PMC article.
Nance-Horan syndrome in females due to a balanced X;1 translocation that disrupts the NHS gene: Familial case report and review of the literature.
Gómez-Laguna L, Martínez-Herrera A, Reyes-de la Rosa ADP, García-Delgado C, Nieto-Martínez K, Fernández-Ramírez F, Valderrama-Atayupanqui TY, Morales-Jiménez AB, Villa-Morales J, Kofman S, Cervantes A, Morán-Barroso VF. Gómez-Laguna L, et al. Ophthalmic Genet. 2018 Jan-Feb;39(1):56-62. doi: 10.1080/13816810.2017.1363245. Epub 2017 Sep 18. Ophthalmic Genet. 2018. PMID: 28922055 Review.