Issue 4/2006
Content (11 Articles)
Current perspectives on the genetic causes of neural tube defects
Patrizia De Marco, Elisa Merello, Samantha Mascelli, Valeria Capra
Genetic susceptibility to Parkinson’s disease among South and North Indians: I. Role of polymorphisms in dopamine receptor and transporter genes and association of DRD4 120-bp duplication marker
Ramesh C. Juyal, Mitashree Das, Sohan Punia, Madhuri Behari, Geetika Nainwal, Sumit Singh, Pazhayannur V. Swaminath, Shyla T. Govindappa, Sachi Jayaram, Uday B. Muthane, B. K Thelma
Familial risks of hospitalization for Parkinson’s disease in first-degree relatives: a nationwide follow-up study from Sweden
Kristina Sundquist, Xinjun Li, Kari Hemminki
Interaction between the dopamine D4 receptor and the serotonin transporter promoter polymorphisms in alcohol and tobacco use among 15-year-olds
M. H. Skowronek, M. Laucht, E. Hohm, K. Becker, M. H. Schmidt
Behavior of mice with mutations in the conserved region deleted in velocardiofacial/DiGeorge syndrome
Jeffrey M. Long, Patricia LaPorte, Sandra Merscher, Birgit Funke, Bruno Saint-Jore, Anne Puech, Raju Kucherlapati, Bernice E. Morrow, Arthur I. Skoultchi, Anthony Wynshaw-Boris
Microcephaly and simplified gyral pattern of the brain associated with early onset insulin-dependent diabetes mellitus
M. C. Y. de Wit, I. F. M. de Coo, C. Julier, M. Delépine, M. H. Lequin, I. van de Laar, B. J. Sibbles, G. J. Bruining, G. M. S. Mancini
Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromes
E. Stogmann, P. Lichtner, C. Baumgartner, M. Schmied, C. Hotzy, F. Asmus, F. Leutmezer, S. Bonelli, E. Assem-Hilger, K. Vass, K. Hatala, T. M. Strom, T. Meitinger, F. Zimprich, A. Zimprich
Spinal muscular atrophy genotyping by gene dosage using multiple ligation-dependent probe amplification
Oronzo Scarciolla, Liborio Stuppia, Maria Vittoria De Angelis, Stefania Murru, Chiara Palka, Rossella Giuliani, Marta Pace, Antonio Di Muzio, Isabella Torrente, Annunziata Morella, Paola Grammatico, Manlio Giacanelli, Maria Cristina Rosatelli, Antonino Uncini, Bruno Dallapiccola
The A431E mutation in PSEN1 causing Familial Alzheimer’s Disease originating in Jalisco State, Mexico: an additional fifteen families
Jill Murrell, Bernardino Ghetti, Elizabeth Cochran, Miguel Angel Macias-Islas, Luis Medina, Arousiak Varpetian, Jeffrey L. Cummings, Mario F. Mendez, Claudia Kawas, Helena Chui, John M. Ringman
Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL
Johanna Annunen-Rasila, Saara Finnilä, Kati Mykkänen, Jukka S. Moilanen, Johanna Veijola, Minna Pöyhönen, Matti Viitanen, Hannu Kalimo, Kari Majamaa