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	1.	Antitumoural activity of a cytotoxic peptide of Lactobacillus casei peptidoglycan and its interaction with mitochondrial-bound hexokinase. [electronic resource] by Fichera, Giuseppe A Fichera, Marco Milone, Giuseppe Producer: 20171020 In: Anti-cancer drugs vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Apneic crises: a clue for MECP2 testing in severe neonatal hypotonia-respiratory failure. [electronic resource] by Falsaperla, Raffaele Pavone, Lorenzo Fichera, Marco Striano, Pasquale Pavone, Piero Producer: 20130307 In: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	An unusual presentation of Becker Nevus. [electronic resource] by Schepis, Carmelo Lentini, Maria Failla, Pinella Castiglia, Lucia Fichera, Marco Romano, Corrado Producer: 20100929 In: European journal of dermatology : EJD vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Hematologic and molecular characterization of a Sicilian cohort of alpha thalassemia carriers. [electronic resource] by Guida, Valentina Colosimo, Alessia Fichera, Marco Lombardo, Turiddu Rigoli, Luciana Dallapiccola, Bruno Producer: 20060824 In: Haematologica vol. 91 Availability: No items available. Save to lists Add to cart (remove)
	5.	Klippel-Trenaunay syndrome in a boy with concomitant ipsilateral overgrowth and undergrowth. [electronic resource] by Ruggieri, Martino Pavone, Vito Polizzi, Agata Falsaperla, Raffaele Fichera, Marco Pavone, Piero Producer: 20150819 In: American journal of medical genetics. Part A vol. 164A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Brief report: peculiar evolution of autistic behaviors in two unrelated children with brachidactyly-mental retardation syndrome. [electronic resource] by Mazzone, Luigi Vassena, Lia Ruta, Liliana Mugno, Diego Galesi, Ornella Fichera, Marco Producer: 20130319 In: Journal of autism and developmental disorders vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Intragenic ILRAPL1 deletion in a male patient with intellectual disability, mild dysmorphic signs, deafness, and behavioral problems. [electronic resource] by Barone, Chiara Bianca, Sebastiano Luciano, Daniela Di Benedetto, Daniela Vinci, Mirella Fichera, Marco Producer: 20160415 In: American journal of medical genetics. Part A vol. 161A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	12q12 deletion: a new patient contributing to genotype-phenotype correlation. [electronic resource] by Failla, Pinella Romano, Corrado Reitano, Santina Di Benedetto, Daniela Grillo, Lucia Fichera, Marco Castiglia, Lucia Producer: 20080528 In: American journal of medical genetics. Part A vol. 146A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	A missense mutation in the coiled-coil domain of the KIF5A gene and late-onset hereditary spastic paraplegia. [electronic resource] by Lo Giudice, Mariangela Neri, Marcella Falco, Michele Sturnio, Maurizio Calzolari, Elisa Di Benedetto, Daniela Fichera, Marco Producer: 20060228 In: Archives of neurology vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Bilateral periventricular nodular heterotopia and lissencephaly in an infant with unbalanced t(12;17)(q24.31; p13.3) translocation. [electronic resource] by Grosso, Salvatore Fichera, Marco Galesi, Ornella Luciano, Daniela Pucci, Lucia Giardini, Francesca Berardi, Rosario Balestri, Paolo Producer: 20080729 In: Developmental medicine and child neurology vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Denaturing HPLC-based assay for molecular screening of nondeletional mutations causing alpha-thalassemias. [electronic resource] by Guida, Valentina Colosimo, Alessia Fiorito, Mirella Foglietta, Enrica Bianco, Ida Ivaldi, Giovanni Fichera, Marco Dallapiccola, Bruno Producer: 20040729 In: Clinical chemistry vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Two novel mutations in the spastin gene (SPG4) found by DHPLC mutation analysis. [electronic resource] by Falco, Michele Scuderi, Carmela Musumeci, Sebastiano Sturnio, Maurizio Neri, Marcella Bigoni, Stefania Caniatti, Luisa Fichera, Marco Producer: 20050131 In: Neuromuscular disorders : NMD vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Severe encephalomyopathy in a patient with homoplasmic A5814G point mutation in mitochondrial tRNACys gene. [electronic resource] by Scuderi, Carmela Borgione, Eugenia Musumeci, Sebastiano Elia, Maurizio Castello, Filippa Fichera, Marco Davidzon, Guido DiMauro, Salvatore Producer: 20070613 In: Neuromuscular disorders : NMD vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	A novel L1CAM mutation in a fetus detected by prenatal diagnosis. [electronic resource] by Piccione, Maria Matina, Federico Fichera, Marco Lo Giudice, Mariangela Damiani, Gianfranca Jakil, Maria Cristina Corsello, Giovanni Producer: 20100520 In: European journal of pediatrics vol. 169 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Denaturing HPLC-based assay for detection of ATRX gene mutations. [electronic resource] by Falco, Michele Luciano, Daniela Sturnio, Maurizio Spalletta, Angela Scionti, Domenico Lo Giudice, Mariangela Romano, Corrado Fichera, Marco Producer: 20050816 In: Clinical chemistry vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Partial monosomy Xq(Xq23 --> qter) and trisomy 4p(4p15.33 --> pter) in a woman with intractable focal epilepsy, borderline intellectual functioning, and dysmorphic features. [electronic resource] by Bartocci, Arnaldo Striano, Pasquale Mancardi, Maria Margherita Fichera, Marco Castiglia, Lucia Galesi, Ornella Michelucci, Roberto Elia, Maurizio Producer: 20080813 In: Brain & development vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	TBR1 is the candidate gene for intellectual disability in patients with a 2q24.2 interstitial deletion. [electronic resource] by Palumbo, Orazio Fichera, Marco Palumbo, Pietro Rizzo, Renata Mazzolla, Elisabetta Cocuzza, Donatella Maria Carella, Massimo Mattina, Teresa Producer: 20141103 In: American journal of medical genetics. Part A vol. 164A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Molecular and clinical characterization of a small duplication Xp in a human female with psychiatric disorders. [electronic resource] by Piccione, Maria Sanfilippo, Cinzia Cavani, Simona Salatiello, Patrizia Malacarne, Michela Pierluigi, Mauro Fichera, Marco Luciano, Daniela Corsello, Giovanni Producer: 20120426 In: Journal of genetics vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Rapid and accurate large-scale genotyping of duplicated genes and discovery of interlocus gene conversions. [electronic resource] by Nuttle, Xander Huddleston, John O'Roak, Brian J Antonacci, Francesca Fichera, Marco Romano, Corrado Shendure, Jay Eichler, Evan E Producer: 20140106 In: Nature methods vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Mutational analysis of the ATRX gene by DGGE: a powerful diagnostic approach for the ATRX syndrome. [electronic resource] by Borgione, Eugenia Sturnio, Maurizio Spalletta, Angela Angela Lo Giudice, Maria Castiglia, Lucia Galesi, Ornella Ragusa, Angela Fichera, Marco Producer: 20030425 In: Human mutation vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 58 results.