Borelina D - Search Results

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Detection of mutations in argentine retinoblastoma patients by segregation of polymorphisms, exon analysis and cytogenetic test.

Dalamon V, Surace E, Borelina D, Ziembar M, Esperante S, Francipane L, Davila M, Parma D, Szijan I. Dalamon V, et al. Among authors: borelina d. Ophthalmic Res. 2001 Nov-Dec;33(6):336-9. doi: 10.1159/000055690. Ophthalmic Res. 2001. PMID: 11721186

Direct deletion analysis in two Duchenne muscular dystrophy symptomatic females using polymorphic dinucleotide (CA)n loci within the dystrophin gene.

Giliberto F, Ferreiro V, Dalamón V, Surace E, Cotignola J, Esperante S, Borelina D, Baranzini S, Szijan I. Giliberto F, et al. Among authors: borelina d. J Biochem Mol Biol. 2003 Mar 31;36(2):179-84. doi: 10.5483/bmbrep.2003.36.2.179. J Biochem Mol Biol. 2003. PMID: 12689516

Combined cytogenetic and molecular analyses for the diagnosis of Prader-Willi/Angelman syndromes.

Borelina D, Engel N, Esperante S, Ferreiro V, Ferrer M, Torrado M, Goldschmidt E, Francipane L, Szijan I. Borelina D, et al. J Biochem Mol Biol. 2004 Sep 30;37(5):522-6. doi: 10.5483/bmbrep.2004.37.5.522. J Biochem Mol Biol. 2004. PMID: 15479613

Clinical, cytogenetic, and molecular testing of Argentine patients with retinoblastoma.

Arbetman A, Abdala M, Fandiño A, Herrera J, Baranzini S, Borelina D, Parma D, Manzitti J, Barreiro C, Giliberto F, Szijan I. Arbetman A, et al. Among authors: borelina d. J AAPOS. 1998 Apr;2(2):102-7. doi: 10.1016/s1091-8531(98)90072-6. J AAPOS. 1998. PMID: 10530971

Supernumerary marker 15 chromosome in a patient with Prader-Willi syndrome.

Borelina D, Esperante S, Gutnisky V, Ferreiro V, Ferrer M, Giliberto F, Frechtel G, Francipane L, Szijan I. Borelina D, et al. Clin Genet. 2004 Mar;65(3):242-3. doi: 10.1111/j.0009-9163.2004.00203.x. Clin Genet. 2004. PMID: 14756675 No abstract available.

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