Pages that link to "Q35247229"
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The following pages link to Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction (Q35247229):
Displaying 50 items.
- Mutation in DHP receptor alpha 1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis (Q24517877) (← links)
- Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome (Q24532354) (← links)
- Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34. (Q24538838) (← links)
- EXT-mutation analysis and loss of heterozygosity in sporadic and hereditary osteochondromas and secondary chondrosarcomas. (Q24540139) (← links)
- Cloning and characterization of the genomic DNA of the human MSSP genes (Q24548175) (← links)
- Polymorphic simple sequence repeat regions in chloroplast genomes: applications to the population genetics of pines (Q24561536) (← links)
- Diversity Arrays Technology (DArT) for whole-genome profiling of barley (Q24561927) (← links)
- Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies (Q24564672) (← links)
- Trinucleotide repeat polymorphism at the human intestinal fatty acid binding protein gene (FABP2) (Q24863851) (← links)
- Dinucleotide repeat polymorphism at the human hemoglobin alpha-1 pseudo-gene (HBAP1) (Q24608456) (← links)
- A mutation in the fibroblast growth factor 14 gene is associated with autosomal dominant cerebellar ataxia [corrected] (Q24615444) (← links)
- AFLP: a new technique for DNA fingerprinting (Q24620887) (← links)
- Dinucleotide repeat polymorphism in the human alpha-cardiac actin gene, intron IV (ACTC), detected using the polymerase chain reaction (Q24624967) (← links)
- Diversity arrays: a solid state technology for sequence information independent genotyping (Q24626746) (← links)
- A locus for autosomal recessive pseudoxanthoma elasticum, with penetrance of vascular symptoms in carriers, maps to chromosome 16p13.1 (Q24628513) (← links)
- Chromosome 7 suppresses indefinite division of nontumorigenic immortalized human fibroblast cell lines KMST-6 and SUSM-1 (Q24629799) (← links)
- Localization of a gene for partial epilepsy to chromosome 10q (Q24646776) (← links)
- Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal dominant form to chromosome 5q (Q24670253) (← links)
- Narrowing the position of the Treacher Collins syndrome locus to a small interval between three new microsatellite markers at 5q32-33.1 (Q24671930) (← links)
- X-linked dominant cone-rod degeneration: linkage mapping of a new locus for retinitis pigmentosa (RP 15) to Xp22.13-p22.11 (Q24672691) (← links)
- The genetic relationship between the Finns and the Finnish Saami (Lapps): analysis of nuclear DNA and mtDNA (Q24675124) (← links)
- Human tritanopia associated with two amino acid substitutions in the blue-sensitive opsin (Q24675989) (← links)
- Map refinement of locus RP13 to human chromosome 17p13.3 in a second family with autosomal dominant retinitis pigmentosa (Q24676387) (← links)
- Genetic mapping of the beta 1 GABA receptor gene to human chromosome 4, using a tetranucleotide repeat polymorphism (Q24678734) (← links)
- A novel mutation in the invariant AG of the acceptor splice site of intron 4 of the beta-hexosaminidase alpha-subunit gene in two unrelated American black GM2-gangliosidosis (Tay-Sachs disease) patients (Q24678854) (← links)
- Molecular genetic basis of maple syrup urine disease in a family with two defective alleles for branched chain acyltransferase and localization of the gene to human chromosome 1 (Q24679357) (← links)
- A novel acropectoral syndrome maps to chromosome 7q36 (Q24680326) (← links)
- Assignment of the mulibrey nanism gene to 17q by linkage and linkage-disequilibrium analysis (Q24680481) (← links)
- SNPSTR: a database of compound microsatellite-SNP markers (Q24684206) (← links)
- SNP frequency, haplotype structure and linkage disequilibrium in elite maize inbred lines (Q24791809) (← links)
- Potential of (GATA)n microsatellites from rice for inter- and intra-specific variability studies (Q24794305) (← links)
- Genetic diversity and relationships in mulberry (genus Morus) as revealed by RAPD and ISSR marker assays (Q24796878) (← links)
- Development of microsatellite markers from an enriched genomic library for genetic analysis of melon (Cucumis melo L.) (Q24805052) (← links)
- Genomic screen for loci associated with tobacco usage in Mission Indians (Q25255604) (← links)
- Genomics of pear and other Rosaceae fruit trees (Q26749129) (← links)
- DNA fingerprinting in zoology: past, present, future (Q26782006) (← links)
- Characterization of the human gene for a newly discovered carbonic anhydrase, CA VII, and its localization to chromosome 16 (Q28115263) (← links)
- Post-genomic era and gene discovery for psychiatric diseases: there is a new art of the trade? The example of the HUMTH01 microsatellite in the Tyrosine Hydroxylase gene (Q28214642) (← links)
- Parental origin of the extra chromosomes in polysomy X (Q28238718) (← links)
- Mapping the human amylase gene cluster on the proximal short arm of chromosome 1 using a highly informative (CA)n repeat (Q28259091) (← links)
- Retroviral and pseudogene insertion sites reveal the lineage of human salivary and pancreatic amylase genes from a single gene during primate evolution (Q28259709) (← links)
- Breakage in the SNRPN locus in a balanced 46,XY,t(15;19) Prader-Willi syndrome patient (Q28292519) (← links)
- A polymorphic (CA)n repeat element maps the human glucokinase gene (GCK) to chromosome 7p (Q28296077) (← links)
- A genome-wide search for genes predisposing to manic-depression, assuming autosomal dominant inheritance (Q28469077) (← links)
- Genetic mapping of a gene causing hypertension in the stroke-prone spontaneously hypertensive rat (Q28565054) (← links)
- Developmental Changes in Morphology of the Middle and Posterior External Cranial Base in Modern Homo sapiens (Q28607805) (← links)
- Clear genetic structure of Pinus kwangtungensis (Pinaceae) revealed by a plastid DNA fragment with a novel minisatellite (Q28752214) (← links)
- Contrasting genetic structures in sister species of North American scrub-jays (Q28765985) (← links)
- Disentangling the genetic determinants of human aging: biological age as an alternative to the use of survival measures (Q28768543) (← links)
- Genetic contribution to biological aging: the Framingham Study (Q28769496) (← links)