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G Cappuccio

Showing results (1-10 of 9) with videos related to

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Applied Optics|April 17, 2010
Photometric linearity test for IR spectrophotometers by means of a rotating sector disk attenuatorG Cappuccio, A D'Amico, S D'Angelo, et al.
Clinical Genetics|March 19, 2013
Identification of two novel splice-site mutations in CHD7 gene in two patients with classical and atypical CHARGE syndrome phenotypeG Cappuccio, V M Ginocchio, A Maffè, et al.
European Journal of Medical Genetics|February 20, 2025
Variability in autism spectrum phenotypes linked to heterozygous missense familial ANK2 mutationR Garotti, M Marino, M P Riccio, et al.
Cardiovascular Surgery (London, England)|October 1, 1994
Embolizing fibroelastoma of the aortic valveT Ragni, A M Grande, G Cappuccio, et al.
Optics Letters|November 28, 2008
Elemental mapping and microimaging by x-ray capillary opticsD Hampai, S B Dabagov, G Cappuccio, et al.
American Journal of Medical Genetics. Part A|October 22, 2019
Expanding the phenotype of DST-related disorder: A case report suggesting a genotype/phenotype correlationG Cappuccio, M Pinelli, A Torella, et al.
Journal of Pediatric Genetics|August 11, 2017
Sensorineural Hearing Loss in a Patient Affected by Congenital Cytomegalovirus Infection: Is It Useful to Identify Comorbid Pathologies?P Fontana, D Melis, A D'Amico, et al.
Minerva Medica|March 21, 2007
[Femoropopliteal arterial thrombosis in a young patient with heterozygous V Leiden factor mutation. Case report]G Cappuccio, R Valesio, V Lamorgese, et al.
Clinical Epigenetics|January 7, 2021
DNA methylation epi-signature is associated with two molecularly and phenotypically distinct clinical subtypes of Phelan-McDermid syndromeL C Schenkel, E Aref-Eshghi, K Rooney, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Applied Optics|April 17, 2010
Photometric linearity test for IR spectrophotometers by means of a rotating sector disk attenuatorG Cappuccio, A D'Amico, S D'Angelo, et al.
Clinical Genetics|March 19, 2013
Identification of two novel splice-site mutations in CHD7 gene in two patients with classical and atypical CHARGE syndrome phenotypeG Cappuccio, V M Ginocchio, A Maffè, et al.
European Journal of Medical Genetics|February 20, 2025
Variability in autism spectrum phenotypes linked to heterozygous missense familial ANK2 mutationR Garotti, M Marino, M P Riccio, et al.
Cardiovascular Surgery (London, England)|October 1, 1994
Embolizing fibroelastoma of the aortic valveT Ragni, A M Grande, G Cappuccio, et al.
Optics Letters|November 28, 2008
Elemental mapping and microimaging by x-ray capillary opticsD Hampai, S B Dabagov, G Cappuccio, et al.
American Journal of Medical Genetics. Part A|October 22, 2019
Expanding the phenotype of DST-related disorder: A case report suggesting a genotype/phenotype correlationG Cappuccio, M Pinelli, A Torella, et al.
Journal of Pediatric Genetics|August 11, 2017
Sensorineural Hearing Loss in a Patient Affected by Congenital Cytomegalovirus Infection: Is It Useful to Identify Comorbid Pathologies?P Fontana, D Melis, A D'Amico, et al.
Minerva Medica|March 21, 2007
[Femoropopliteal arterial thrombosis in a young patient with heterozygous V Leiden factor mutation. Case report]G Cappuccio, R Valesio, V Lamorgese, et al.
Clinical Epigenetics|January 7, 2021
DNA methylation epi-signature is associated with two molecularly and phenotypically distinct clinical subtypes of Phelan-McDermid syndromeL C Schenkel, E Aref-Eshghi, K Rooney, et al.
Pageof 1