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Page 1
Genetic Analysis Algorithm for the Study of Patients with Multiple Congenital Anomalies and Isolated Congenital Heart Disease.
Genes (Basel). 2022 Jun 29;13(7):1172. doi: 10.3390/genes13071172.
Genes (Basel). 2022.
PMID: 35885957
Free PMC article.
Genetic Imbalances in Argentinean Patients with Congenital Conotruncal Heart Defects.
Delea M, Espeche LD, Bruque CD, Bidondo MP, Massara LS, Oliveri J, Brun P, Cosentino VR, Martinoli C, Tolaba N, Picon C, Ponce Zaldua ME, Ávila S, Gutnisky V, Perez M, Furforo L, Buzzalino ND, Liascovich R, Groisman B, Rittler M, Rozental S, Barbero P, Dain L.
Delea M, et al. Among authors: brun p.
Genes (Basel). 2018 Sep 11;9(9):454. doi: 10.3390/genes9090454.
Genes (Basel). 2018.
PMID: 30208644
Free PMC article.
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Detection of critical congenital heart disease among newborns in Argentina through the national surveillance system of congenital heart disease (RENAC).
Groisman B, Barbero P, Liascovich R, Brun P, Bidondo MP.
Groisman B, et al. Among authors: brun p.
Arch Argent Pediatr. 2022 Feb;120(1):6-13. doi: 10.5546/aap.2022.eng.6. Epub 2021 Dec 3.
Arch Argent Pediatr. 2022.
PMID: 35068114
Free article.
English, Spanish.
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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: brun p.
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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[Clinical diagnosis of Kabuki syndrome: phenotype and associated abnormalities in two new cases].
Andersen MS, Menazzi S, Brun P, Cocah C, Merla G, Solari A.
Andersen MS, et al. Among authors: brun p.
Arch Argent Pediatr. 2014 Feb;112(1):e13-e17. doi: 10.5546/aap.2014.e13.
Arch Argent Pediatr. 2014.
PMID: 24566779
Free article.
Spanish.
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