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D Milani

Showing results (61-70 of 65) with videos related to

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Environmental Pollution (Barking, Essex : 1987)|June 11, 2017
Effect of substituted phenylamine antioxidants on three life stages of the freshwater mussel Lampsilis siliquoideaR S Prosser, P L Gillis, E A M Holman, et al.
Clinical Genetics|January 31, 2014
Clinical and molecular characterization of Rubinstein-Taybi syndrome patients carrying distinct novel mutations of the EP300 geneG Negri, D Milani, P Colapietro, et al.
Epigenetics|September 18, 2018
Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disordersL Fontana, M F Bedeschi, S Maitz, et al.
Clinical Genetics|February 10, 2016
Fetal growth patterns in Beckwith-Wiedemann syndromeA Mussa, S Russo, A de Crescenzo, et al.
American Journal of Medical Genetics. Part A|March 3, 2005
Mutation analysis of the NSD1 gene in a group of 59 patients with congenital overgrowthM Cecconi, F Forzano, D Milani, et al.
Pageof 7

Showing results (61-70 of 65) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 65 results.
Environmental Pollution (Barking, Essex : 1987)|June 11, 2017
Effect of substituted phenylamine antioxidants on three life stages of the freshwater mussel Lampsilis siliquoideaR S Prosser, P L Gillis, E A M Holman, et al.
Clinical Genetics|January 31, 2014
Clinical and molecular characterization of Rubinstein-Taybi syndrome patients carrying distinct novel mutations of the EP300 geneG Negri, D Milani, P Colapietro, et al.
Epigenetics|September 18, 2018
Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disordersL Fontana, M F Bedeschi, S Maitz, et al.
Clinical Genetics|February 10, 2016
Fetal growth patterns in Beckwith-Wiedemann syndromeA Mussa, S Russo, A de Crescenzo, et al.
American Journal of Medical Genetics. Part A|March 3, 2005
Mutation analysis of the NSD1 gene in a group of 59 patients with congenital overgrowthM Cecconi, F Forzano, D Milani, et al.
Pageof 7