Showing results (91-100 of 956) with videos related to

Sort By:
Pageof 96
Neurogenetics|March 15, 2008
Further examination of the candidate genes in chromosome 12p13 locus for late-onset Alzheimer diseaseJoseph H Lee, Rong Cheng, Ekaterina Rogaeva, et al.
Neurogenetics|January 15, 2008
Suggestive evidence for linkage for restless legs syndrome on chromosome 19p13David Kemlink, Giuseppe Plazzi, Roberto Vetrugno, et al.
Neurogenetics|March 7, 2008
Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish populationBeyhan Tüysüz, Fatih Bayrakli, Michael L DiLuna, et al.
Neurogenetics|August 31, 2006
Current perspectives on the genetic causes of neural tube defectsPatrizia De Marco, Elisa Merello, Samantha Mascelli, et al.
Neurogenetics|October 18, 2006
Identification of two novel mutations and of a novel critical region in the KRIT1 geneVito Guarnieri, Lucia A Muscarella, Rosina Amoroso, et al.
Neurogenetics|July 4, 2006
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 markerRamesh C Juyal, Mitashree Das, Sohan Punia, et al.
Neurogenetics|April 7, 2007
Evaluation of autism traits in Angelman syndrome: a resource to unfold autism genesMaria Teresa Bonati, Silvia Russo, Palma Finelli, et al.
Neurogenetics|June 17, 2006
Molecular mechanism of rigid spine with muscular dystrophy type 1 caused by novel mutations of selenoprotein N geneYuji Okamoto, Hiroshi Takashima, Itsuro Higuchi, et al.
Neurogenetics|June 20, 2008
Characterization of novel CAPN3 isoforms in white blood cells: an alternative approach for limb-girdle muscular dystrophy 2A diagnosisL Blázquez, M Azpitarte, A Sáenz, et al.
Neurogenetics|March 30, 2004
Mutations of the MTHFR gene (428C>T and [458G>T+459C>T]) markedly decrease MTHFR enzyme activityHidetaka Yano, Kazuhiro Nakaso, Kenichi Yasui, et al.
Pageof 96