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M C Digilio

Showing results (121-130 of 130) with videos related to

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Clinical Genetics|December 6, 2012
Syndromic non-compaction of the left ventricle: associated chromosomal anomaliesM C Digilio, L Bernardini, M G Gagliardi, et al.
Clinical Genetics|November 2, 2011
Novel and recurrent JAG1 mutations in patients with tetralogy of FallotV Guida, F Chiappe, R Ferese, et al.
International Journal of Cancer|October 23, 2001
Ext-mutation analysis in Italian sporadic and hereditary osteochondromasM Gigante, M G Matera, D Seripa, et al.
Minerva Pediatrica|November 26, 2009
[Multidisciplinary approach]A Bartuli, E Bertini, F Callea, et al.
Clinical Genetics|October 2, 2009
Mild ring 17 syndrome shares common phenotypic features irrespective of the chromosomal breakpoints locationC Surace, S Piazzolla, P Sirleto, et al.
Genes, Brain, and Behavior|April 6, 2017
Visual perception skills: a comparison between patients with Noonan syndrome and 22q11.2 deletion syndromeG Piccini, D Menghini, A D'Andrea, et al.
Journal of Intellectual Disability Research : JIDR|June 15, 2011
Needs and challenges of daily life for people with Down syndrome residing in the city of Rome, ItalyM Bertoli, G Biasini, M T Calignano, et al.
Clinical Genetics|September 1, 2017
Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndromeM Niceta, K Margiotti, M C Digilio, et al.
Medrxiv : the Preprint Server for Health Sciences|October 7, 2024
Identifying individuals at risk for surgical supravalvar aortic stenosis by polygenic risk score with graded phenotypingD Liu, C B Mervis, M D Levin, et al.
Circulation|July 25, 2000
Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defectsS Giglio, S L Graw, G Gimelli, et al.
Pageof 13

Showing results (121-130 of 130) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 130 results.
Clinical Genetics|December 6, 2012
Syndromic non-compaction of the left ventricle: associated chromosomal anomaliesM C Digilio, L Bernardini, M G Gagliardi, et al.
Clinical Genetics|November 2, 2011
Novel and recurrent JAG1 mutations in patients with tetralogy of FallotV Guida, F Chiappe, R Ferese, et al.
International Journal of Cancer|October 23, 2001
Ext-mutation analysis in Italian sporadic and hereditary osteochondromasM Gigante, M G Matera, D Seripa, et al.
Minerva Pediatrica|November 26, 2009
[Multidisciplinary approach]A Bartuli, E Bertini, F Callea, et al.
Clinical Genetics|October 2, 2009
Mild ring 17 syndrome shares common phenotypic features irrespective of the chromosomal breakpoints locationC Surace, S Piazzolla, P Sirleto, et al.
Genes, Brain, and Behavior|April 6, 2017
Visual perception skills: a comparison between patients with Noonan syndrome and 22q11.2 deletion syndromeG Piccini, D Menghini, A D'Andrea, et al.
Journal of Intellectual Disability Research : JIDR|June 15, 2011
Needs and challenges of daily life for people with Down syndrome residing in the city of Rome, ItalyM Bertoli, G Biasini, M T Calignano, et al.
Clinical Genetics|September 1, 2017
Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndromeM Niceta, K Margiotti, M C Digilio, et al.
Medrxiv : the Preprint Server for Health Sciences|October 7, 2024
Identifying individuals at risk for surgical supravalvar aortic stenosis by polygenic risk score with graded phenotypingD Liu, C B Mervis, M D Levin, et al.
Circulation|July 25, 2000
Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defectsS Giglio, S L Graw, G Gimelli, et al.
Pageof 13