Pages that link to "Q42767488"

The following pages link to Jonathan Peter Warner (Q42767488):

Displaying 23 items.

• Organization of the human glucokinase regulator gene GCKR (Q24312789) (← links)
• Analysis of chromosome 21 copy number in uncultured amniocytes by fluorescence in situ hybridization using a cosmid contig (Q31046133) (← links)
• Spinocerebellar ataxia type 8 in Scotland: frequency, neurological, neuropsychological and neuropsychiatric findings (Q31140629) (← links)
• Emery-Dreifuss muscular dystrophy: linkage to markers in distal Xq28. (Q33863959) (← links)
• A study of the Huntington's disease associated trinucleotide repeat in the Scottish population. (Q33596076) (← links)
• P67L: a cystic fibrosis allele with mild effects found at high frequency in the Scottish population. (Q33680182) (← links)
• Spinocerebellar ataxia type 8 in Scotland: genetic and clinical features in seven unrelated cases and a review of published reports. (Q35480115) (← links)
• BRCA1 5382insC mutation in sporadic and familial breast and ovarian carcinoma in Scotland (Q36431727) (← links)
• Divergent effects of cannabidiol on the discriminative stimulus and place conditioning effects of Delta(9)-tetrahydrocannabinol (Q36517347) (← links)
• Structural analysis of the human ret proto-oncogene using exon trapping. (Q36768151) (← links)
• Discriminative stimulus properties of delta9-tetrahydrocannabinol (THC) in C57Bl/6J mice (Q37339113) (← links)
• Targeted sequencing of the Paget's disease associated 14q32 locus identifies several missense coding variants in RIN3 that predispose to Paget's disease of bone. (Q40453402) (← links)
• Human glucokinase regulatory protein (GCKR): cDNA and genomic cloning, complete primary structure, and chromosomal localization. (Q41314089) (← links)
• Improved PCR based methods for detecting C9orf72 hexanucleotide repeat expansions. (Q41951834) (← links)
• A general method for the detection of large CAG repeat expansions by fluorescent PCR (Q42028239) (← links)
• A novel atypical 22q11.2 distal deletion in father and son. (Q43075032) (← links)
• A single allele from the polymorphic CCG rich sequence immediately 3' to the unstable CAG trinucleotide in the IT15 cDNA shows almost complete disequilibrium with Huntington's disease chromosomes in the Scottish population (Q45289993) (← links)
• A new polymerase chain reaction (PCR) assay for the trinucleotide repeat that is unstable and expanded on Huntington's disease chromosomes (Q45290738) (← links)
• The ASP1 gene of Saccharomyces cerevisiae, encoding the intracellular isozyme of L-asparaginase (Q48081625) (← links)
• A human parthenogenetic chimaera (Q52205845) (← links)
• Molecular genetics of the human glucokinase regulator-fructokinase (GCKR-KHK) region of chromosome 2p23. (Q54571433) (← links)
• Co-localization of the ketohexokinase and glucokinase regulator genes to a 500-kb region of Chromosome 2p23 (Q56459580) (← links)
• Chromosomal organisation of a repeated gene cluster expressed in mammalian stages of Leishmania (Q64447381) (← links)