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Hematological Oncology|September 24, 2004
High sensitivity of chemiluminescent methodology for detection of clonal CDR3 sequences in patients with acute lymphoblastic leukemiaE Leal, A R Jaloma-Cruz, P Barros-NúñezAnnales De Genetique|January 1, 1997
High recurrence of recombinants in a family with pericentric inversion of chromosome 18G Mejía-Baltodano, L Bobadilla, R M Gonzalez, et al.Neurologia|August 26, 2015
Evolution and genomics of the human brainM A Rosales-Reynoso, C I Juárez-Vázquez, P Barros-NúñezClinical Genetics|October 16, 2007
Crouzon with acanthosis nigricans. Further delineation of the syndromeL Arnaud-López, R Fragoso, J Mantilla-Capacho, et al.Revista De Neurologia|July 15, 2009
[Diseases caused by triplet expansion]M A Rosales-Reynoso, A B Ochoa-Hernández, P Barros-NúñezGenetic Counseling (Geneva, Switzerland)|January 31, 2006
Apert syndrome with preaxial polydactyly showing the typical mutation Ser252Trp in the FGFR2 geneJ M Mantilla-Capacho, L Arnaud, M Díaz-Rodriguez, et al.Genetic Counseling (Geneva, Switzerland)|February 5, 2011
Variegated-like mosaicism and ring syndrome in a r(4) boy. Appraisal of 38 patients with a fairly complete ring 4M G Domínguez, P Barros-Núñez, I A González-Ramos, et al.Neurologia (Barcelona, Spain)|September 14, 2014
Epigenetic mechanisms in the development of memory and their involvement in certain neurological diseasesM A Rosales-Reynoso, A B Ochoa-Hernández, C I Juárez-Vázquez, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1997
A familial syndrome with hypotonia, mental retardation and dysmorphic features resembling Cohen syndromeG Mejía-Baltodano, L Bobadilla, A Solís, et al.Sangre|October 1, 1991
[Fetal hemoglobin in children with different neoplasms]B Ibarra, J Montes, C Becerra, et al.Pageof 3