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Pietro Sirleto

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Oncology Letters|January 27, 2017
Sometimes it is better to wait: First Italian case of a newborn with transient abnormal myelopoiesis and a favorable prognosisGuglielmo Salvatori, Silvia Foligno, Pietro Sirleto, et al.
Oncotarget|July 9, 2014
Usp7 protects genomic stability by regulating Bub3Serena Giovinazzi, Pietro Sirleto, Vasilisa Aksenova, et al.
Orphanet Journal of Rare Diseases|January 15, 2016
Role of molecular testing in the multidisciplinary diagnostic approach of ichthyosisAndrea Diociaiuti, May El Hachem, Elisa Pisaneschi, et al.
BMC Medical Genetics|September 4, 2015
CHARGE syndrome due to deletion of region upstream of CHD7 gene START codonElisa Pisaneschi, Pietro Sirleto, Francesca Romana Lepri, et al.
Virchows Archiv : an International Journal of Pathology|February 3, 2009
RABGAP1L gene rearrangement resulting from a der(Y)t(Y;1)(q12;q25) in acute myeloid leukemia arising in a child with Klinefelter syndromeMaria Cristina Roberti, Roberta La Starza, Cecilia Surace, et al.
Pediatric Research|December 19, 2008
Lyonization effects of the t(X;16) translocation on the phenotypic expression in a rare female with Menkes diseasePietro Sirleto, Cecilia Surace, Helena Santos, et al.
Pediatric Neurology|April 16, 2014
Epilepsy in patients with duplications of chromosome 14 harboring FOXG1Giuseppe Pontrelli, Simona Cappelletti, Dianela Claps, et al.
Cancer Genetics|January 14, 2014
Two novel cases of trilateral retinoblastoma: genetics and review of the literatureGemma D'Elia, Simona Grotta, Francesca Del Bufalo, et al.
Orphanet Journal of Rare Diseases|April 21, 2011
Complex chromosome rearrangements related 15q14 microdeletion plays a relevant role in phenotype expression and delineates a novel recurrent syndromeMaria Cristina Roberti, Cecilia Surace, Maria Cristina Digilio, et al.
Clinical Biochemistry|May 4, 2011
Characterization of a novel isolated deletion of the exon 3 within the CFTR gene: Relevance for phenotypic expression and genetic counselingAnna Cristina Tomaiuolo, Pietro Sirleto, Claudia Centrone, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Oncology Letters|January 27, 2017
Sometimes it is better to wait: First Italian case of a newborn with transient abnormal myelopoiesis and a favorable prognosisGuglielmo Salvatori, Silvia Foligno, Pietro Sirleto, et al.
Oncotarget|July 9, 2014
Usp7 protects genomic stability by regulating Bub3Serena Giovinazzi, Pietro Sirleto, Vasilisa Aksenova, et al.
Orphanet Journal of Rare Diseases|January 15, 2016
Role of molecular testing in the multidisciplinary diagnostic approach of ichthyosisAndrea Diociaiuti, May El Hachem, Elisa Pisaneschi, et al.
BMC Medical Genetics|September 4, 2015
CHARGE syndrome due to deletion of region upstream of CHD7 gene START codonElisa Pisaneschi, Pietro Sirleto, Francesca Romana Lepri, et al.
Virchows Archiv : an International Journal of Pathology|February 3, 2009
RABGAP1L gene rearrangement resulting from a der(Y)t(Y;1)(q12;q25) in acute myeloid leukemia arising in a child with Klinefelter syndromeMaria Cristina Roberti, Roberta La Starza, Cecilia Surace, et al.
Pediatric Research|December 19, 2008
Lyonization effects of the t(X;16) translocation on the phenotypic expression in a rare female with Menkes diseasePietro Sirleto, Cecilia Surace, Helena Santos, et al.
Pediatric Neurology|April 16, 2014
Epilepsy in patients with duplications of chromosome 14 harboring FOXG1Giuseppe Pontrelli, Simona Cappelletti, Dianela Claps, et al.
Cancer Genetics|January 14, 2014
Two novel cases of trilateral retinoblastoma: genetics and review of the literatureGemma D'Elia, Simona Grotta, Francesca Del Bufalo, et al.
Orphanet Journal of Rare Diseases|April 21, 2011
Complex chromosome rearrangements related 15q14 microdeletion plays a relevant role in phenotype expression and delineates a novel recurrent syndromeMaria Cristina Roberti, Cecilia Surace, Maria Cristina Digilio, et al.
Clinical Biochemistry|May 4, 2011
Characterization of a novel isolated deletion of the exon 3 within the CFTR gene: Relevance for phenotypic expression and genetic counselingAnna Cristina Tomaiuolo, Pietro Sirleto, Claudia Centrone, et al.
Pageof 3