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Vincenzo Antona

Showing results (1-10 of 57) with videos related to

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Urology|June 5, 2016
Genetic Basis of Posterior Urethral Valves InheritanceCinzia Chiaramonte, Denisia Bommarito, Elisa Zambaiti, et al.
Italian Journal of Pediatrics|November 10, 2019
NF1 microdeletion syndrome: case report of two new patientsGregorio Serra, Vincenzo Antona, Giovanni Corsello, et al.
Clinical Case Reports|February 16, 2018
Esophageal atresia and Beckwith-Wiedemann syndrome in one of the naturally conceived discordant newborn twins: first reportGregorio Serra, Vincenzo Antona, Mandy Schierz, et al.
American Journal of Medical Genetics. Part A|October 15, 2013
PTEN hamartoma tumor syndromes in childhood: description of two cases and a proposal for follow-up protocolMaria Piccione, Tiziana Fragapane, Vincenzo Antona, et al.
American Journal of Medical Genetics. Part A|April 5, 2014
Response to Stanich et al.: Correspondence regarding-PTEN hamartoma tumor syndromes in childhood-Description of two cases and a proposal for follow-up protocolMaria Piccione, Tiziana Fragapane, Vincenzo Antona, et al.
BMC Medical Genomics|April 9, 2021
A paradigmatic autistic phenotype associated with loss of PCDH11Y and NLGN4Y genesRosaria Nardello, Vincenzo Antona, Giuseppe Donato Mangano, et al.
Clinical Dysmorphology|May 21, 2020
Infant developmental profile of Crisponi syndrome due to compound heterozygosity for CRLF1 deletionIngrid Anne Mandy Schierz, Gregorio Serra, Vincenzo Antona, et al.
European Journal of Pediatrics|January 21, 2010
Array CGH defined interstitial deletion on chromosome 14: a new caseMaria Piccione, Vincenzo Antona, Valeria Scavone, et al.
Italian Journal of Pediatrics|June 17, 2021
Novel SCNN1A gene splicing-site mutation causing autosomal recessive pseudohypoaldosteronism type 1 (PHA1) in two Italian patients belonging to the same small townGregorio Serra, Vincenzo Antona, Maria Michela D'Alessandro, et al.
Italian Journal of Pediatrics|July 2, 2021
Jacobsen syndrome and neonatal bleeding: report on two unrelated patientsGregorio Serra, Luigi Memo, Vincenzo Antona, et al.
Pageof 6

Showing results (1-10 of 57) with videos related to

Sort By:
Pageof 6
Urology|June 5, 2016
Genetic Basis of Posterior Urethral Valves InheritanceCinzia Chiaramonte, Denisia Bommarito, Elisa Zambaiti, et al.
Italian Journal of Pediatrics|November 10, 2019
NF1 microdeletion syndrome: case report of two new patientsGregorio Serra, Vincenzo Antona, Giovanni Corsello, et al.
Clinical Case Reports|February 16, 2018
Esophageal atresia and Beckwith-Wiedemann syndrome in one of the naturally conceived discordant newborn twins: first reportGregorio Serra, Vincenzo Antona, Mandy Schierz, et al.
American Journal of Medical Genetics. Part A|October 15, 2013
PTEN hamartoma tumor syndromes in childhood: description of two cases and a proposal for follow-up protocolMaria Piccione, Tiziana Fragapane, Vincenzo Antona, et al.
American Journal of Medical Genetics. Part A|April 5, 2014
Response to Stanich et al.: Correspondence regarding-PTEN hamartoma tumor syndromes in childhood-Description of two cases and a proposal for follow-up protocolMaria Piccione, Tiziana Fragapane, Vincenzo Antona, et al.
BMC Medical Genomics|April 9, 2021
A paradigmatic autistic phenotype associated with loss of PCDH11Y and NLGN4Y genesRosaria Nardello, Vincenzo Antona, Giuseppe Donato Mangano, et al.
Clinical Dysmorphology|May 21, 2020
Infant developmental profile of Crisponi syndrome due to compound heterozygosity for CRLF1 deletionIngrid Anne Mandy Schierz, Gregorio Serra, Vincenzo Antona, et al.
European Journal of Pediatrics|January 21, 2010
Array CGH defined interstitial deletion on chromosome 14: a new caseMaria Piccione, Vincenzo Antona, Valeria Scavone, et al.
Italian Journal of Pediatrics|June 17, 2021
Novel SCNN1A gene splicing-site mutation causing autosomal recessive pseudohypoaldosteronism type 1 (PHA1) in two Italian patients belonging to the same small townGregorio Serra, Vincenzo Antona, Maria Michela D'Alessandro, et al.
Italian Journal of Pediatrics|July 2, 2021
Jacobsen syndrome and neonatal bleeding: report on two unrelated patientsGregorio Serra, Luigi Memo, Vincenzo Antona, et al.
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