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Francesca R Grati

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Epigenetics|April 27, 2010
Epigenetic modulation of the IGF2/H19 imprinted domain in human embryonic and extra-embryonic compartments and its possible role in fetal growth restrictionSilvia Tabano, Patrizia Colapietro, Irene Cetin, et al.
European Journal of Human Genetics : EJHG|January 19, 2006
Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villiFrancesca R Grati, Beatrice Grimi, Giuditia Frascoli, et al.
American Journal of Medical Genetics. Part A|June 16, 2005
Three cases with de novo 6q imbalance and variable prenatal phenotypeFrancesca R Grati, Faustina Lalatta, Licia Turolla, et al.
European Journal of Cancer (Oxford, England : 1990)|November 14, 2012
X chromosome inactivation pattern in BRCA gene mutation carriersSiranoush Manoukian, Paolo Verderio, Silvia Tabano, et al.
Prenatal Diagnosis|October 23, 2016
Frequency of fetal karyotype abnormalities in women undergoing invasive testing in the absence of ultrasound and other high-risk indicationsJose Carlos P Ferreira, Francesca R Grati, Komal Bajaj, et al.
American Journal of Medical Genetics. Part A|April 9, 2009
Pure monosomy and pure trisomy of 13q21.2-31.1 consequent to a familial insertional translocation: exclusion of PCDH9 as the responsible gene for autosomal dominant auditory neuropathy (AUNA1)Francesca R Grati, Marci M Lesperance, Simona De Toffol, et al.
Cytogenetic and Genome Research|December 10, 2015
Cryptic 13q34 and 4q35.2 Deletions in an Italian FamilyFederica Riccardi, Gianna F Rivolta, Vera Uliana, et al.
Journal of Immunology (Baltimore, Md. : 1950)|June 24, 2005
X chromosome monosomy: a common mechanism for autoimmune diseasesPietro Invernizzi, Monica Miozzo, Carlo Selmi, et al.
Molecular and Cellular Probes|July 29, 2008
Prenatal detection by subtelomeric FISH and MLPA of unbalanced meiotic recombinants resulting from parental pericentric inversionsFrancesca R Grati, Sara Chinetti, Roberta Malgara, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 15, 2014
Fetoplacental mosaicism: potential implications for false-positive and false-negative noninvasive prenatal screening resultsFrancesca R Grati, Francesca Malvestiti, Jose C P B Ferreira, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Epigenetics|April 27, 2010
Epigenetic modulation of the IGF2/H19 imprinted domain in human embryonic and extra-embryonic compartments and its possible role in fetal growth restrictionSilvia Tabano, Patrizia Colapietro, Irene Cetin, et al.
European Journal of Human Genetics : EJHG|January 19, 2006
Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villiFrancesca R Grati, Beatrice Grimi, Giuditia Frascoli, et al.
American Journal of Medical Genetics. Part A|June 16, 2005
Three cases with de novo 6q imbalance and variable prenatal phenotypeFrancesca R Grati, Faustina Lalatta, Licia Turolla, et al.
European Journal of Cancer (Oxford, England : 1990)|November 14, 2012
X chromosome inactivation pattern in BRCA gene mutation carriersSiranoush Manoukian, Paolo Verderio, Silvia Tabano, et al.
Prenatal Diagnosis|October 23, 2016
Frequency of fetal karyotype abnormalities in women undergoing invasive testing in the absence of ultrasound and other high-risk indicationsJose Carlos P Ferreira, Francesca R Grati, Komal Bajaj, et al.
American Journal of Medical Genetics. Part A|April 9, 2009
Pure monosomy and pure trisomy of 13q21.2-31.1 consequent to a familial insertional translocation: exclusion of PCDH9 as the responsible gene for autosomal dominant auditory neuropathy (AUNA1)Francesca R Grati, Marci M Lesperance, Simona De Toffol, et al.
Cytogenetic and Genome Research|December 10, 2015
Cryptic 13q34 and 4q35.2 Deletions in an Italian FamilyFederica Riccardi, Gianna F Rivolta, Vera Uliana, et al.
Journal of Immunology (Baltimore, Md. : 1950)|June 24, 2005
X chromosome monosomy: a common mechanism for autoimmune diseasesPietro Invernizzi, Monica Miozzo, Carlo Selmi, et al.
Molecular and Cellular Probes|July 29, 2008
Prenatal detection by subtelomeric FISH and MLPA of unbalanced meiotic recombinants resulting from parental pericentric inversionsFrancesca R Grati, Sara Chinetti, Roberta Malgara, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 15, 2014
Fetoplacental mosaicism: potential implications for false-positive and false-negative noninvasive prenatal screening resultsFrancesca R Grati, Francesca Malvestiti, Jose C P B Ferreira, et al.
Pageof 3