Grüters, A.

family chromosome deletion mutation sequence chorea protein marker thyroid region genomic 200 control chromosomes disorder factor analysis genetic chromosome 14 q chromosome 14 family uk 1 transcription basal function patient disease development basal ganglia result individual primer position study movement 11. thyroid transcription factor family nl 1 allele families nl 1 g 713t 1.2 mb neuron genomic deletion pcr products c 727a university r 243s ganglia onset database cycle transcript product 2.1 homeodomain codon genet huntington domain genbank family members choreic movements abnormality g 303fsx department member extension 5 min exon 3_ b binding 1.2 breedveld symptom evidence str markers person ii -4 figure bac c -2577n bhc patient iii -1. thyroid dysfunction g-to-t base change signal