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Maria Piccione

Showing results (11-20 of 74) with videos related to

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The Italian Journal of Biochemistry|December 18, 2003
Aminoacid profile and oxidative status in children affected by Down syndrome before and after supplementary nutritional treatmentMarcello Ciaccio, Maria Piccione, Mario Giuffrè, et al.
European Journal of Pediatrics|January 21, 2010
Array CGH defined interstitial deletion on chromosome 14: a new caseMaria Piccione, Vincenzo Antona, Valeria Scavone, et al.
American Journal of Medical Genetics. Part A|July 29, 2003
Abnormalities of the umbilico-portal venous system in Down syndrome: a report of two new patientsSalvatore Pipitone, Caterina Garofalo, Giovanni Corsello, et al.
Italian Journal of Pediatrics|July 30, 2020
12q14.3 microdeletion involving HMGA2 gene cause a Silver-Russell syndrome-like phenotype: a case report and review of the literatureFrancesca Mercadante, Martina Busè, Emanuela Salzano, et al.
European Journal of Pediatrics|December 11, 2008
Q289P mutation in the FGFR2 gene: first report in a patient with type 1 Pfeiffer syndromeMaria Piccione, Vincenzo Antona, Marcello Niceta, et al.
Journal of Genetics|June 17, 2011
Deletion of NSD1 exon 14 in Sotos syndrome: first descriptionMaria Piccione, Valeria Consiglio, Antonella Di Fiore, et al.
American Journal of Medical Genetics. Part A|July 18, 2009
Identification of two new mutations in TRPS 1 gene leading to the tricho-rhino-phalangeal syndrome type I and IIIMaria Piccione, Marcello Niceta, Vincenzo Antona, et al.
European Journal of Pediatrics|August 18, 2009
A novel L1CAM mutation in a fetus detected by prenatal diagnosisMaria Piccione, Federico Matina, Marco Fichera, et al.
American Journal of Medical Genetics. Part A|January 27, 2010
Array-CGH defined chromosome 1p duplication in a patient with autism spectrum disorder, mild mental deficiency, and minor dysmorphic featuresMaria Piccione, Vincenzo Antona, Roberta Antona, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 15, 2015
4p16.1-p15.31 duplication and 4p terminal deletion in a 3-years old Chinese girl: Array-CGH, genotype-phenotype and neurological characterizationMaria Piccione, Emanuela Salzano, Davide Vecchio, et al.
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Showing results (11-20 of 74) with videos related to

Sort By:
Pageof 8
The Italian Journal of Biochemistry|December 18, 2003
Aminoacid profile and oxidative status in children affected by Down syndrome before and after supplementary nutritional treatmentMarcello Ciaccio, Maria Piccione, Mario Giuffrè, et al.
European Journal of Pediatrics|January 21, 2010
Array CGH defined interstitial deletion on chromosome 14: a new caseMaria Piccione, Vincenzo Antona, Valeria Scavone, et al.
American Journal of Medical Genetics. Part A|July 29, 2003
Abnormalities of the umbilico-portal venous system in Down syndrome: a report of two new patientsSalvatore Pipitone, Caterina Garofalo, Giovanni Corsello, et al.
Italian Journal of Pediatrics|July 30, 2020
12q14.3 microdeletion involving HMGA2 gene cause a Silver-Russell syndrome-like phenotype: a case report and review of the literatureFrancesca Mercadante, Martina Busè, Emanuela Salzano, et al.
European Journal of Pediatrics|December 11, 2008
Q289P mutation in the FGFR2 gene: first report in a patient with type 1 Pfeiffer syndromeMaria Piccione, Vincenzo Antona, Marcello Niceta, et al.
Journal of Genetics|June 17, 2011
Deletion of NSD1 exon 14 in Sotos syndrome: first descriptionMaria Piccione, Valeria Consiglio, Antonella Di Fiore, et al.
American Journal of Medical Genetics. Part A|July 18, 2009
Identification of two new mutations in TRPS 1 gene leading to the tricho-rhino-phalangeal syndrome type I and IIIMaria Piccione, Marcello Niceta, Vincenzo Antona, et al.
European Journal of Pediatrics|August 18, 2009
A novel L1CAM mutation in a fetus detected by prenatal diagnosisMaria Piccione, Federico Matina, Marco Fichera, et al.
American Journal of Medical Genetics. Part A|January 27, 2010
Array-CGH defined chromosome 1p duplication in a patient with autism spectrum disorder, mild mental deficiency, and minor dysmorphic featuresMaria Piccione, Vincenzo Antona, Roberta Antona, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 15, 2015
4p16.1-p15.31 duplication and 4p terminal deletion in a 3-years old Chinese girl: Array-CGH, genotype-phenotype and neurological characterizationMaria Piccione, Emanuela Salzano, Davide Vecchio, et al.
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