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Orsetta Zuffardi

Showing results (1-10 of 222) with videos related to

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European Journal of Medical Genetics|June 20, 2022
The embryo battle against adverse genomes: Are de novo terminal deletions the rescue of unfavorable zygotic imbalances?Orsetta Zuffardi, Marco Fichera, Maria Clara Bonaglia
Seminars in Fetal & Neonatal Medicine|January 7, 2011
Array technology in prenatal diagnosisOrsetta Zuffardi, Annalisa Vetro, Paul Brady, et al.
Epilepsia|July 31, 2007
Scotosensitive and photosensitive myoclonic seizures in an infant with trisomy 13Claudia Torniero, Orsetta Zuffardi, Francesca Darra, et al.
American Journal of Medical Genetics. Part A|December 8, 2005
A 46,X,inv(Y) young woman with gonadal dysgenesis and gonadoblastoma: cytogenetics, molecular, and methylation studiesGiorgio Gimelli, Roberto Giorda, Silvana Beri, et al.
American Journal of Medical Genetics. Part A|December 14, 2006
A patient with duplication (7)(p22.1pter) characterized by array-CGHLaila Zahed, Tiziano Pramparo, Chantal Farra, et al.
Human Pathology|June 17, 2011
Correlation between genomic alterations assessed by array comparative genomic hybridization, prognostically informative histologic subtype, stage, and patient survival in gastric cancerElena Rossi, Catherine Klersy, Rachele Manca, et al.
Acta Diabetologica|November 6, 2014
Wolfram syndrome 2: a novel CISD2 mutation identified in Italian siblingsMaurizio Rondinelli, Francesca Novara, Valeria Calcaterra, et al.
Prenatal Diagnosis|March 5, 2011
Current controversies in prenatal diagnosis 3: is conventional chromosome analysis necessary in the post-array CGH era?The-Hung Bui, Annalisa Vetro, Orsetta Zuffardi, et al.
European Journal of Medical Genetics|September 24, 2005
Narrowing the deleted region associated with the 15q21 syndromeTiziano Pramparo, Teresa Mattina, Stefania Gimelli, et al.
European Journal of Pediatrics|January 27, 2017
Developmental trends of communicative skills in children with chromosome 14 aberrationsLaura Zampini, Paola Zanchi, Berardo Rinaldi, et al.
Pageof 23

Showing results (1-10 of 222) with videos related to

Sort By:
Pageof 23
European Journal of Medical Genetics|June 20, 2022
The embryo battle against adverse genomes: Are de novo terminal deletions the rescue of unfavorable zygotic imbalances?Orsetta Zuffardi, Marco Fichera, Maria Clara Bonaglia
Seminars in Fetal & Neonatal Medicine|January 7, 2011
Array technology in prenatal diagnosisOrsetta Zuffardi, Annalisa Vetro, Paul Brady, et al.
Epilepsia|July 31, 2007
Scotosensitive and photosensitive myoclonic seizures in an infant with trisomy 13Claudia Torniero, Orsetta Zuffardi, Francesca Darra, et al.
American Journal of Medical Genetics. Part A|December 8, 2005
A 46,X,inv(Y) young woman with gonadal dysgenesis and gonadoblastoma: cytogenetics, molecular, and methylation studiesGiorgio Gimelli, Roberto Giorda, Silvana Beri, et al.
American Journal of Medical Genetics. Part A|December 14, 2006
A patient with duplication (7)(p22.1pter) characterized by array-CGHLaila Zahed, Tiziano Pramparo, Chantal Farra, et al.
Human Pathology|June 17, 2011
Correlation between genomic alterations assessed by array comparative genomic hybridization, prognostically informative histologic subtype, stage, and patient survival in gastric cancerElena Rossi, Catherine Klersy, Rachele Manca, et al.
Acta Diabetologica|November 6, 2014
Wolfram syndrome 2: a novel CISD2 mutation identified in Italian siblingsMaurizio Rondinelli, Francesca Novara, Valeria Calcaterra, et al.
Prenatal Diagnosis|March 5, 2011
Current controversies in prenatal diagnosis 3: is conventional chromosome analysis necessary in the post-array CGH era?The-Hung Bui, Annalisa Vetro, Orsetta Zuffardi, et al.
European Journal of Medical Genetics|September 24, 2005
Narrowing the deleted region associated with the 15q21 syndromeTiziano Pramparo, Teresa Mattina, Stefania Gimelli, et al.
European Journal of Pediatrics|January 27, 2017
Developmental trends of communicative skills in children with chromosome 14 aberrationsLaura Zampini, Paola Zanchi, Berardo Rinaldi, et al.
Pageof 23