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Genetic Imbalances in Argentinean Patients with Congenital Conotruncal Heart Defects.
Genes (Basel). 2018 Sep 11;9(9):454. doi: 10.3390/genes9090454.
Genes (Basel). 2018.
PMID: 30208644
Free PMC article.
Genetic Analysis Algorithm for the Study of Patients with Multiple Congenital Anomalies and Isolated Congenital Heart Disease.
Delea M, Massara LS, Espeche LD, Bidondo MP, Barbero P, Oliveri J, Brun P, Fabro M, Galain M, Fernández CS, Taboas M, Bruque CD, Kolomenski JE, Izquierdo A, Berenstein A, Cosentino V, Martinoli C, Vilas M, Rittler M, Mendez R, Furforo L, Liascovich R, Groisman B, Rozental S, Dain L, On Behalf Of The Pid Acm-Cc Group.
Delea M, et al. Among authors: furforo l.
Genes (Basel). 2022 Jun 29;13(7):1172. doi: 10.3390/genes13071172.
Genes (Basel). 2022.
PMID: 35885957
Free PMC article.
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Proximal trisomy 1q in a girl with developmental delay and minor anomalies.
Furforo L, Rittler M, Slavutsky IR.
Furforo L, et al.
Am J Med Genet. 1996 Sep 6;64(4):551-5. doi: 10.1002/(SICI)1096-8628(19960906)64:4<551::AID-AJMG5>3.0.CO;2-S.
Am J Med Genet. 1996.
PMID: 8870921
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Double Autosomal/Gonosomal Mosaic Trisomy 47,XXX/47,XX,+14 in a Newborn with Multiple Congenital Anomalies.
Massara LS, Delea M, Espeche L, Bruque CD, Oliveri J, Brun P, Furforo L, Dain L, Rozental S.
Massara LS, et al. Among authors: furforo l.
Cytogenet Genome Res. 2019;159(3):137-142. doi: 10.1159/000504238. Epub 2019 Nov 30.
Cytogenet Genome Res. 2019.
PMID: 31786569
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A der(11)t(4;11)(q21;p15) in a T-ALL/LBL patient.
Colli S, Furforo L, Rojo Pisarello E, Maidana M, Martín C, Bordone J, Slavutsky I.
Colli S, et al. Among authors: furforo l.
Cancer Genet. 2016 Apr;209(4):166-70. doi: 10.1016/j.cancergen.2016.01.001. Epub 2016 Jan 12.
Cancer Genet. 2016.
PMID: 26883452
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