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- A genome-wide association study of sporadic ALS in a homogenous Irish population Journal Articles
- An efficient strategy for gene mapping using multipoint linkage analysis: exclusion of the multiple endocrine neoplasia 2A (MEN2A) locus from chromosome 13. Journal Articles
- Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4) Journal Articles
- Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3. Journal Articles
- Genome scan of Arab Israeli families maps a schizophrenia susceptibility gene to chromosome 6q23 and supports a locus at chromosome 10q24 Journal Articles
- Linkage analysis of 26 Canadian breast and breast-ovarian cancer families Journal Articles
- Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2A. Journal Articles
- Mapping autism risk loci using genetic linkage and chromosomal rearrangements Journal Articles
- Mutation of the slow myosin heavy chain rod domain underlies hyaline body myopathy Journal Articles
- Paramyotonia congenita and hyperkalemic periodic paralysis are linked to the adult muscle sodium channel gene Journal Articles
- Quebec platelet disorder is linked to the urokinase plasminogen activator gene (PLAU) and increases expression of the linked allele in megakaryocytes Journal Articles
- Recombination between the factor VIII gene and the DXS52 locus gives the most probable genetic order as centromere‐FRA(X)‐DXS15‐DXS52‐F8C‐telomere Journal Articles
- The Genetic Distance between the Coagulation Factor IX Gene and the Locus for the Fragile X Syndrome: Clinical Implications Journal Articles
- [Search for 22q11 deletion and linkage study in familial cases of non-syndromic conotruncal defects]. Journal Articles