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S Giglio

Showing results (31-40 of 73) with videos related to

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American Journal of Medical Genetics. Part A|November 5, 2003
Ring chromosome 10 (p15q26) in a patient with unipolar affective disorder, multiple minor anomalies, and mental retardationD Concolino, M A Iembo, M T Moricca, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 3, 2015
Proton nuclear magnetic resonance spectroscopy of urine samples in preterm asphyctic newborn: a metabolomic approachM Longini, S Giglio, S Perrone, et al.
Psychopharmacology|January 1, 1985
Effect of metergoline on human anxietyF G Graeff, A W Zuardi, J S Giglio, et al.
Journal of Medical Genetics|March 19, 2002
Familial pericentric inversion of chromosome 5 in a family with benign neonatal convulsionsD Concolino, M A Iembo, E Rossi, et al.
Oncogene|August 11, 2010
Regulation of MDM4 (MDMX) function by p76(MDM2): a new facet in the control of p53 activityS Giglio, F Mancini, M Pellegrino, et al.
American Journal of Medical Genetics|December 18, 2001
Inv dup del (1)(pter-->q44::q44-->q42:) with the classical phenotype of trisomy 1q42-qterD De Brasi, E Rossi, S Giglio, et al.
Human Genetics|June 1, 1997
Ataxic gait and mental retardation with absence of the paternal chromosome 8 and an idic(8)(p23.3): imprinting effect or nullisomy for distal 8p genes?M Piantanida, C Dellavecchia, G Floridia, et al.
American Journal of Medical Genetics. Part A|February 25, 2003
De novo double translocation 3;13 and 4;8;18 in a patient with mental retardation and skeletal abnormalitiesC Battisti, M C Bonaglia, S Giglio, et al.
The Journal of Infection|September 18, 2020
Serum Ferritin is an independent risk factor for Acute Respiratory Distress Syndrome in COVID-19O Gandini, A Criniti, L Ballesio, et al.
Genetic Counseling (Geneva, Switzerland)|December 3, 2015
MYOCLONIC ASTATIC EPILEPSY IN A PATIENT WITH A DE NOVO 4q21.22q21.23 MICRODUPLICATIONV Ottaviani, A Bartocci, M Pantaleo, et al.
Pageof 8

Showing results (31-40 of 73) with videos related to

Sort By:
Pageof 8
American Journal of Medical Genetics. Part A|November 5, 2003
Ring chromosome 10 (p15q26) in a patient with unipolar affective disorder, multiple minor anomalies, and mental retardationD Concolino, M A Iembo, M T Moricca, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 3, 2015
Proton nuclear magnetic resonance spectroscopy of urine samples in preterm asphyctic newborn: a metabolomic approachM Longini, S Giglio, S Perrone, et al.
Psychopharmacology|January 1, 1985
Effect of metergoline on human anxietyF G Graeff, A W Zuardi, J S Giglio, et al.
Journal of Medical Genetics|March 19, 2002
Familial pericentric inversion of chromosome 5 in a family with benign neonatal convulsionsD Concolino, M A Iembo, E Rossi, et al.
Oncogene|August 11, 2010
Regulation of MDM4 (MDMX) function by p76(MDM2): a new facet in the control of p53 activityS Giglio, F Mancini, M Pellegrino, et al.
American Journal of Medical Genetics|December 18, 2001
Inv dup del (1)(pter-->q44::q44-->q42:) with the classical phenotype of trisomy 1q42-qterD De Brasi, E Rossi, S Giglio, et al.
Human Genetics|June 1, 1997
Ataxic gait and mental retardation with absence of the paternal chromosome 8 and an idic(8)(p23.3): imprinting effect or nullisomy for distal 8p genes?M Piantanida, C Dellavecchia, G Floridia, et al.
American Journal of Medical Genetics. Part A|February 25, 2003
De novo double translocation 3;13 and 4;8;18 in a patient with mental retardation and skeletal abnormalitiesC Battisti, M C Bonaglia, S Giglio, et al.
The Journal of Infection|September 18, 2020
Serum Ferritin is an independent risk factor for Acute Respiratory Distress Syndrome in COVID-19O Gandini, A Criniti, L Ballesio, et al.
Genetic Counseling (Geneva, Switzerland)|December 3, 2015
MYOCLONIC ASTATIC EPILEPSY IN A PATIENT WITH A DE NOVO 4q21.22q21.23 MICRODUPLICATIONV Ottaviani, A Bartocci, M Pantaleo, et al.
Pageof 8