Authors:
THOMAS P
WILKINSON F
NGUYEN TM
HARPER PS
NEAL JW
MORRIS GE
JONES AL
Citation: P. Thomas et al., FULL-LENGTH HUNTINGTIN IS NOT DETECTED IN INTRANUCLEAR INCLUSIONS IN HUNTINGTONS-DISEASE BRAIN, European journal of human genetics, 6, 1998, pp. 4187-4187
Authors:
PHILLIPS MF
ROGERS MT
BARNETSON R
BRAUN C
HARLEY HG
MYRING J
STEVENS D
WILES CM
HARPER PS
Citation: Mf. Phillips et al., PROMM - THE EXPANDING PHENOTYPE - A FAMILY WITH PROXIMAL MYOPATHY, MYOTONIA AND DEAFNESS, Neuromuscular disorders, 8(7), 1998, pp. 439-446
Authors:
THOMAS P
WILKINSON F
MAN NT
HARPER PS
NEAL JW
MORRIS GE
JONES AL
Citation: P. Thomas et al., FULL-LENGTH HUNTINGTIN IS NOT DETECTED IN INTRANUCLEAR INCLUSIONS IN HUNTINGTONS-DISEASE BRAIN, Biochemical Society transactions, 26(3), 1998, pp. 243-243
Authors:
SINGHRAO SK
THOMAS P
WOOD JD
MACMILLAN JC
NEAL JW
HARPER PS
JONES AL
Citation: Sk. Singhrao et al., HUNTINGTIN PROTEIN COLOCALIZES WITH LESIONS OF NEURODEGENERATIVE DISEASES - AN INVESTIGATION IN HUNTINGTONS, ALZHEIMERS, AND PICKS DISEASES, Experimental neurology, 150(2), 1998, pp. 213-222
Citation: Ps. Harper, GENETIC TESTING, LIFE-INSURANCE, AND ADVERSE SELECTION, Philosophical transactions-Royal Society of London. Biological sciences, 352(1357), 1997, pp. 1063-1066
Authors:
BECHER MW
RUBINSZTEIN DC
LEGGO J
WAGSTER MV
STINE OC
RANEN NG
FRANZ ML
ABBOTT MH
SHERR M
MACMILLAN JC
BARRON L
PORTEOUS M
HARPER PS
ROSS CA
Citation: Mw. Becher et al., DENTATORUBRAL AND PALLIDOLUYSIAN ATROPHY (DRPLA) - CLINICAL AND NEUROPATHOLOGICAL FINDINGS IN GENETICALLY CONFIRMED NORTH-AMERICAN AND EUROPEAN PEDIGREES, Movement disorders, 12(4), 1997, pp. 519-530
Citation: Al. Jones et al., HUNTINGTON-DISEASE - ADVANCES IN MOLECULAR AND CELL BIOLOGY, Journal of inherited metabolic disease, 20(2), 1997, pp. 125-138
Authors:
UPADHYAYA M
MAYNARD J
ROGERS MT
LUNT PW
JARDINE P
RAVINE D
HARPER PS
Citation: M. Upadhyaya et al., IMPROVED MOLECULAR DIAGNOSIS OF FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY (FSHD) - VALIDATION OF THE DIFFERENTIAL DOUBLE DIGESTION FOR FSHD, Journal of Medical Genetics, 34(6), 1997, pp. 476-479
Citation: M. Rogers et al., DEVELOPMENT OF A CLINICAL PROTOCOL FOR USE IN CLINICAL-TRIALS AND ONGOING ASSESSMENT AND MANAGEMENT IN MYOTONIC-DYSTROPHY, Journal of Medical Genetics, 34, 1997, pp. 547-547
Citation: S. Verhoef et Ps. Harper, INFANTILE HUNTINGTONS-DISEASE WITH AN UNUSUALLY LARGE CAG EXPANSION, Journal of Medical Genetics, 34, 1997, pp. 553-553
Authors:
PAYNE Y
WILLIAMS M
CHEADLE J
STOTT NCH
ROWLANDS M
SHICKLE D
WEST G
MEREDITH L
GOODCHILD M
HARPER PS
CLARKE A
Citation: Y. Payne et al., CARRIER SCREENING FOR CYSTIC-FIBROSIS IN PRIMARY-CARE - EVALUATION OFA PROJECT IN SOUTH WALES, Clinical genetics, 51(3), 1997, pp. 153-163
Citation: J. Scourfield et al., HUNTINGTONS-DISEASE - PSYCHIATRIC PRACTICE IN MOLECULAR-GENETIC PREDICTION AND DIAGNOSIS, British Journal of Psychiatry, 170, 1997, pp. 146-149
Citation: Al. Jones et al., 2 PROTEINS WHICH INTERACT WITH THE N-TERMINUS OF HUNTINGTIN, American journal of human genetics, 61(4), 1997, pp. 1819-1819
Authors:
SINGHRAO SK
THOMAS P
WOOD JD
HARPER PS
NEAL JW
JONES AL
Citation: Sk. Singhrao et al., HUNTINGTIN IS ASSOCIATED WITH INTRACELLULAR NEUROPATHOLOGY IN HUNTINGTONS, ALZHEIMERS AND PICKS-DISEASE, American journal of human genetics, 61(4), 1997, pp. 1877-1877
Citation: Jm. Boutell et al., GENERATION OF CLONES WITH VARYING TRINUCLEOTIDE REPEAT SIRES USING INTRINSIC INSTABILITY IN E-COLI, American journal of human genetics, 61(4), 1997, pp. 2368-2368