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2. FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, México. Issue 6 (1st May 2019)

3. Hydroxyurea induces chromosomal damage in G2 and enhances the clastogenic effect of mitomycin C in Fanconi anemia cells. (6th February 2015)

4. Interstitial deletion of 2q24.2: Further delineation of an emerging syndrome associated with intellectual disability, severe hypotonia and moderate intrauterine growth restriction. Issue 3 (19th December 2013)

5. Low bone mineral density and renal malformation in Mexican patients with Turner syndrome are associated with single nucleotide variants in vitamin D-metabolism genes. (2nd September 2019)