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L Garavelli

Showing results (111-120 of 116) with videos related to

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Italian Journal of Pediatrics|March 11, 2018
Prematurity, ventricular septal defect and dysmorphisms are independent predictors of pathogenic copy number variants: a retrospective study on array-CGH results and phenotypical features of 293 children with neurodevelopmental disorders and/or multiple congenital anomaliesI Maini, I Ivanovski, O Djuric, et al.
American Journal of Medical Genetics. Part A|September 19, 2009
Mandibuloacral dysplasia type A in childhoodL Garavelli, M R D'Apice, F Rivieri, et al.
Neuropediatrics|December 7, 2007
Megalencephaly and perisylvian polymicrogyria with postaxial polydactyly and hydrocephalus (MPPH): report of a new caseL Garavelli, E Guareschi, S Errico, et al.
Clinical Genetics|December 17, 2015
Expanding the clinical spectrum of the 'HDAC8-phenotype' - implications for molecular diagnostics, counseling and risk predictionI Parenti, C Gervasini, J Pozojevic, et al.
American Journal of Medical Genetics. Part A|February 14, 2009
Mowat-Wilson syndrome: facial phenotype changing with age: study of 19 Italian patients and review of the literatureL Garavelli, M Zollino, P Cerruti Mainardi, et al.
Leukemia & Lymphoma|July 29, 2016
Hodgkin's Disease in 50 Intravenous Drug Users with HIV-InfectionS Monfardini, U Tirelli, E Vaccher, et al.
Pageof 12

Showing results (111-120 of 116) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 116 results.
Italian Journal of Pediatrics|March 11, 2018
Prematurity, ventricular septal defect and dysmorphisms are independent predictors of pathogenic copy number variants: a retrospective study on array-CGH results and phenotypical features of 293 children with neurodevelopmental disorders and/or multiple congenital anomaliesI Maini, I Ivanovski, O Djuric, et al.
American Journal of Medical Genetics. Part A|September 19, 2009
Mandibuloacral dysplasia type A in childhoodL Garavelli, M R D'Apice, F Rivieri, et al.
Neuropediatrics|December 7, 2007
Megalencephaly and perisylvian polymicrogyria with postaxial polydactyly and hydrocephalus (MPPH): report of a new caseL Garavelli, E Guareschi, S Errico, et al.
Clinical Genetics|December 17, 2015
Expanding the clinical spectrum of the 'HDAC8-phenotype' - implications for molecular diagnostics, counseling and risk predictionI Parenti, C Gervasini, J Pozojevic, et al.
American Journal of Medical Genetics. Part A|February 14, 2009
Mowat-Wilson syndrome: facial phenotype changing with age: study of 19 Italian patients and review of the literatureL Garavelli, M Zollino, P Cerruti Mainardi, et al.
Leukemia & Lymphoma|July 29, 2016
Hodgkin's Disease in 50 Intravenous Drug Users with HIV-InfectionS Monfardini, U Tirelli, E Vaccher, et al.
Pageof 12