subject area of
- A genome-wide association study of sporadic ALS in a homogenous Irish population Academic Article
- An efficient strategy for gene mapping using multipoint linkage analysis: exclusion of the multiple endocrine neoplasia 2A (MEN2A) locus from chromosome 13. Academic Article
- Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4) Academic Article
- Genome scan of Arab Israeli families maps a schizophrenia susceptibility gene to chromosome 6q23 and supports a locus at chromosome 10q24 Academic Article
- Genome-wide Linkage Analysis for Severe Obesity in French Caucasians Finds Significant Susceptibility Locus on Chromosome 19q Academic Article
- Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2A. Academic Article
- Mapping autism risk loci using genetic linkage and chromosomal rearrangements Academic Article
- Mutation of the slow myosin heavy chain rod domain underlies hyaline body myopathy Academic Article
- Paramyotonia congenita and hyperkalemic periodic paralysis are linked to the adult muscle sodium channel gene Academic Article
- Quebec platelet disorder is linked to the urokinase plasminogen activator gene (PLAU) and increases expression of the linked allele in megakaryocytes Academic Article
- Recombination between the factor VIII gene and the DXS52 locus gives the most probable genetic order as centromere-FRA(X)-DXS15-DXS52-F8C-telomere Academic Article
- [Search for 22q11 deletion and linkage study in familial cases of non-syndromic conotruncal defects]. Academic Article