Pages that link to "Q40556170"

The following pages link to Isolation and mapping of a polymorphic DNA sequence (pMCT118) on chromosome 1p [D1S80] (Q40556170):

Displaying 24 items.

• Maternal uniparental isodisomy of chromosome 14: association with autosomal recessive rod monochromacy (Q24670101) (← links)
• DNA typing of a polymerase chain reaction amplified D1S80/amelogenin multiplex using capillary electrophoresis and a mixed entangled polymer matrix (Q30469593) (← links)
• Fixed-bin analysis for statistical evaluation of continuous distributions of allelic data from VNTR loci, for use in forensic comparisons (Q31042608) (← links)
• Combined karyotyping, CGH and M-FISH analysis allows detailed characterization of unidentified chromosomal rearrangements in Merkel cell carcinoma (Q34810928) (← links)
• An exclusion map for pre-eclampsia: assuming autosomal recessive inheritance (Q35195615) (← links)
• Analysis of the VNTR locus D1S80 by the PCR followed by high-resolution PAGE (Q35195894) (← links)
• Laboratory and field evaluation of polymerase chain reaction-based forensic DNA profiling for use in identification of human blood meal sources of Aedes aegypti (Diptera: Culicidae). (Q40617681) (← links)
• A new sequenced allelic ladder marker for D1S80 typing (Q48203026) (← links)
• Mutation at the human D1S80 minisatellite locus (Q51336008) (← links)
• The distribution of HLA DQA1 and D1S80 (pMCT118) alleles and genotypes in the populations of Galicia and central Portugal. (Q52807799) (← links)
• Specificity of genetic diversity in D1S80 revealed by SNP-VNTR haplotyping. (Q54354501) (← links)
• A HinfI polymorphism in the 5' flanking region of the human VNTR locus D1S80. (Q54394303) (← links)
• Genetic variability at the D1S80 minisatellite: predominance of allele 18 among some indian populations. (Q54677896) (← links)
• Deletion mapping of chromosome 1p and 22q in pheochromocytoma. (Q55037406) (← links)
• Polymorphisms at locus D1S80 and other hypervariable regions in the analysis of Eastern European ethnic group relationships (Q58135557) (← links)
• Rehydratable gels: a potential reference standard support for electrophoresing PCR-amplified DNA (Q67527692) (← links)
• Suitability of PCR methods for forensic investigation. Analysis of the 3'apoB VNTR system in an Italian population sample (Q67840094) (← links)
• Simple protocols for typing forensic biological evidence: chemiluminescent detection for human DNA quantitation and restriction fragment length polymorphism (RFLP) analyses and manual typing of polymerase chain reaction (PCR) amplified polymorphisms (Q70953223) (← links)
• Allelic imbalance on chromosome 1 in human breast cancer. I. Minisatellite and RFLP analysis (Q71680202) (← links)
• Allele frequency distribution of the D1S80 (pMCT118) locus polymorphism in the Japanese population by the polymerase chain reaction (Q72266278) (← links)
• Hinf I/Tsp509 I and BsoF I polymorphisms in the flanking regions of the human VNTR locus D1S80 (Q73041996) (← links)
• Paternity testing by the detection of D1S80 VNTR using fluorescence image analyzer (Dualcolour system) (Q73043846) (← links)
• Nucleotide substitution in the 5′ flanking region of D1S80 locus (Q73720092) (← links)
• DNA sequence analysis of long PCR amplified products at the D1S80 locus (Q73846926) (← links)