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Archives of Medical Research|July 1, 1997
Cytogenetic findings in 303 Mexican patients with de novo acute myeloblastic leukemiaR M Arana-Trejo, E Gómez-Morales, M E Rubio-Borja, et al.European Journal of Pediatrics|February 7, 1998
Favourable clinical course in an infant with severe deficiency of complex III of the respiratory chain combined with less severe deficiencies of complexes I, II and IVM E Rubio-Gozalbo, W Ruitenbeek, H A Bentlage, et al.Annals of Hematology|August 20, 2002
Intermediate doses of melphalan and dexamethasone are better than vincristine, adriamycin, and dexamethasone (VAD) and polychemotherapy for the treatment of primary plasma cell leukemiaJ Vela-Ojeda, M A García-Ruiz Esparza, A Rosas-Cabral, et al.European Journal of Medical Genetics|December 11, 2012
Adducted thumbs: a clinical clue to genetic diagnosisJ M A Verhagen, C T R M Schrander-Stumpel, M M J Blezer, et al.Annals of Neurology|June 9, 1999
Leigh syndrome associated with a mutation in the NDUFS7 (PSST) nuclear encoded subunit of complex IR H Triepels, L P van den Heuvel, J L Loeffen, et al.Annals of Neurology|June 14, 2000
Clinical and biochemical characteristics of congenital disorder of glycosylation type Ic, the first recognized endoplasmic reticulum defect in N-glycan synthesisS Grünewald, T Imbach, K Huijben, et al.Clinical and Laboratory Haematology|June 18, 2002
BCR/ABL p210, p190 and p230 fusion genes in 250 Mexican patients with chronic myeloid leukaemia (CML)R M Arana-Trejo, E Ruíz Sánchez, G Ignacio-Ibarra, et al.Journal of Medical Genetics|May 6, 2008
Termination of damaged protein repair defines the occurrence of symptoms in carriers of the m.3243A > G tRNA(Leu) mutationR G E van Eijsden, L M T Eijssen, P J Lindsey, et al.Orphanet Journal of Rare Diseases|May 19, 2016
Childhood Pompe disease: clinical spectrum and genotype in 31 patientsC I van Capelle, J C van der Meijden, J M P van den Hout, et al.Nucleosides, Nucleotides & Nucleic Acids|June 15, 2010
Dihydropyrimidine dehydrogenase deficiency caused by a novel genomic deletion c.505_513del of DPYDA B P van Kuilenburg, J Meijer, G Gökcay, et al.Pageof 7