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Genetic Epidemiology|December 22, 1999
The importance of watching our weights: how the choice of weights for non-independent sib pairs can dramatically alter resultsP Van Eerdewegh, J Dupuis, S L Santangelo, et al.
BMC Genetics|February 21, 2004
A QTL genome scan of the metabolic syndrome and its component traitsMatthew B McQueen, Lars Bertram, Eric B Rimm, et al.
Annali Italiani Di Chirurgia|February 28, 2002
[Functional results of colorectal and coloanal anastomosis with and without pouch]M Santangelo, G Romano, G Vescio, et al.
Cardiologia (Rome, Italy)|April 1, 1994
[Double ventricular response to a single atrial stimulation caused by simultaneous anterograde conduction through two atrioventricular nodal pathways]P Vitale, L Santangelo, M S Mayer, et al.
HPB Surgery : a World Journal of Hepatic, Pancreatic and Biliary Surgery|March 27, 1998
Cystic dilation of extrahepatic bile ducts in adulthood: diagnosis, surgical treatment and long-term resultsG Belli, G Rotondano, A D'Agostino, et al.
Genetic Epidemiology|January 1, 1997
Probabilistic diagnosis in linkage analysis of bipolar disorder: putting weights on the fringeP Van Eerdewegh, S L Santangelo, H Lee, et al.
Cardiologia (Rome, Italy)|June 1, 1993
[Linking in a phase-3 branch block: the electrocardiographic manifestations]P Vitale, L Santangelo, C Nave, et al.
Giornale Italiano Di Medicina Del Lavoro Ed Ergonomia|April 16, 2008
[Electromagnetic interference of electronic devices in workers with AICD]G Inserra, R Barletta, L Santangelo, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 9, 2011
Common genetic variation in the GAD1 gene and the entire family of DLX homeobox genes and autism spectrum disordersShun-Chiao Chang, David L Pauls, Christoph Lange, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 18, 2013
Sex-specific association of a common variant of the XG gene with autism spectrum disordersShun-Chiao Chang, David L Pauls, Christoph Lange, et al.
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