Works matching IS 13646745 AND DT 2006 AND VI 7 AND IP 4
Results: 11
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.
- Published in:
- Neurogenetics, 2006, v. 7, n. 4, p. 223, doi. 10.1007/s10048-006-0048-y
- By:
- Publication type:
- Article
Interaction between the dopamine D4 receptor and the serotonin transporter promoter polymorphisms in alcohol and tobacco use among 15-year-olds.
- Published in:
- Neurogenetics, 2006, v. 7, n. 4, p. 239, doi. 10.1007/s10048-006-0050-4
- By:
- Publication type:
- Article
Spinal muscular atrophy genotyping by gene dosage using multiple ligation-dependent probe amplification.
- Published in:
- Neurogenetics, 2006, v. 7, n. 4, p. 269, doi. 10.1007/s10048-006-0051-3
- By:
- Publication type:
- Article
The A431E mutation in PSEN1 causing Familial Alzheimer’s Disease originating in Jalisco State, Mexico: an additional fifteen families.
- Published in:
- Neurogenetics, 2006, v. 7, n. 4, p. 277, doi. 10.1007/s10048-006-0053-1
- By:
- Publication type:
- Article
Behavior of mice with mutations in the conserved region deleted in velocardiofacial/DiGeorge syndrome.
- Published in:
- Neurogenetics, 2006, v. 7, n. 4, p. 247, doi. 10.1007/s10048-006-0054-0
- By:
- Publication type:
- Article
Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromes.
- Published in:
- Neurogenetics, 2006, v. 7, n. 4, p. 265, doi. 10.1007/s10048-006-0057-x
- By:
- Publication type:
- Article
Current perspectives on the genetic causes of neural tube defects.
- Published in:
- Neurogenetics, 2006, v. 7, n. 4, p. 201, doi. 10.1007/s10048-006-0052-2
- By:
- Publication type:
- Article
Familial risks of hospitalization for Parkinson’s disease in first-degree relatives: a nationwide follow-up study from Sweden.
- Published in:
- Neurogenetics, 2006, v. 7, n. 4, p. 231, doi. 10.1007/s10048-006-0055-z
- By:
- Publication type:
- Article
Microcephaly and simplified gyral pattern of the brain associated with early onset insulin-dependent diabetes mellitus.
- Published in:
- Neurogenetics, 2006, v. 7, n. 4, p. 259, doi. 10.1007/s10048-006-0061-1
- By:
- Publication type:
- Article
Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL.
- Published in:
- 2006
- By:
- Publication type:
- Correction Notice
Acknowledgement to Referees 2005–2006.
- Published in:
- Neurogenetics, 2006, v. 7, n. 4, p. 283, doi. 10.1007/s10048-006-0064-y
- Publication type:
- Article