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	1.	A Genomic and Epigenomic Approach for Studying Neuropsychiatric Disorders Associated to Early-life Stress: Part II. [electronic resource] by Pappalardo, Xena Giada Cavallaro, Sebastiano Publication details: Current genomics Dec 2018 In: Current genomics vol. 19 Availability: No items available. Save to lists Add to cart (remove)
	2.	Editorial: A Genomic and Epigenomic Approach for Studying Neuropsychiatric Disorders Associated to Early-life Stress: Part I. [electronic resource] by Pappalardo, Xena Giada Cavallaro, Sebastiano Publication details: Current genomics Nov 2018 In: Current genomics vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Child Abuse Syndrome (CAS): A Newly Recognized Distinct Entity. [electronic resource] by Parano, Enrico Pappalardo, Xena Giada Pavone, Piero Ruggieri, Martino Cavallaro, Sebastiano Producer: 20160808 In: The open neurology journal vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation? [electronic resource] by Pavone, Piero Corsello, Giovanni Cho, Sung Yoon Pappalardo, Xena Giada Ruggieri, Martino Marino, Simona Domenica Jin, Dong Kyu Marino, Silvia Falsaperla, Raffaele Producer: 20200527 In: Italian journal of pediatrics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Previously Unreported [electronic resource] by Venti, Valeria Scalia, Bruna Sauna, Alessandra Nasca, Maria Rita Smilari, Pierluigi Praticò, Andrea D Fiumara, Agata Pappalardo, Xena G Pavone, Piero Publication details: Molecular syndromology Jan 2020 In: Molecular syndromology vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Chromosome 15q BP3 to BP5 deletion is a likely locus for speech delay and language impairment: Report on a four-member family and an unrelated boy. [electronic resource] by Pavone, Piero Ruggieri, Martino Marino, Simona D Corsello, Giovanni Pappalardo, Xena Polizzi, Agata Parano, Enrico Romano, Catia Marino, Silvia Praticò, Andrea Domenico Falsaperla, Raffaele Producer: 20210402 In: Molecular genetics & genomic medicine vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)