Syndromes with lissencephalyPILZ, D. T; QUARRELL, O. W. J.Journal of medical genetics. 1996, Vol 33, Num 4, pp 319-323, issn 0022-2593Article

Evidence for possible Mendelian inheritance of septo-optic dysplasiaWALES, J. K. H; QUARRELL, O. W. J.Acta paediatrica (Oslo). 1996, Vol 85, Num 3, pp 391-392, issn 0803-5253Article

Huntington's disease: prediction and preventionHARPER, P. S; QUARRELL, O. W. J; YOUNGMAN, S et al.Philosophical transactions of the Royal Society of London. Series B, Biological sciences. 1988, Vol 319, Num 1194, pp 285-298, issn 0080-4622Conference Paper

Liver histology in the arthrogryposis multiplex congenita, renal dysfunction, and cholestasis (ARC) syndrome : report of three new cases and reviewHORSLEN, S. P; QUARRELL, O. W. J; TANNER, M. S et al.Journal of medical genetics. 1994, Vol 31, Num 1, pp 62-64, issn 0022-2593Article

Maxillonasal dysplasia (Binder's syndrome)QUARRELL, O. W. J; KOCH, M; HUGHES, H. E et al.Journal of medical genetics. 1990, Vol 27, Num 6, pp 384-387, issn 0022-2593Article

Pallister-killian mosaic syndrome with emphasis on the adult phenotypeQUARRELL, O. W. J; HAMILL, M. A; HUGHES, H. E et al.American journal of medical genetics. 1988, Vol 31, Num 6, pp 841-844, issn 0148-7299Article

Schinzel-Giedion syndrome : Evidence for a neurodegenerative processSHAH, A. M; SMITH, M. F; GRIFFITHS, P. D et al.American journal of medical genetics. 1999, Vol 82, Num 4, pp 344-347, issn 0148-7299Article

An integrated microcomputer system to maintain a genetic register for Huntington diseaseMANSOOR SARFARAZI; QUARRELL, O. W. J; WOLAK, G et al.American journal of medical genetics. 1987, Vol 28, Num 4, pp 999-1006, issn 0148-7299Article

An epidemiological study of Wolf-Hirschhorn syndrome : life expectancy and cause of mortalitySHANNON, N. L; MALTBY, E. L; RIGBY, A. S et al.Journal of medical genetics. 2001, Vol 38, Num 10, pp 674-679, issn 0022-2593Article

Population studies of Huntington's disease in WalesQUARRELL, O. W. J; TYLER, A; JONES, M. P et al.Clinical genetics. 1988, Vol 33, Num 3, pp 189-195, issn 0009-9163Article

Absence of close linkage between benign hereditary chorea and the locus D4S10 (probe G8)QUARRELL, O. W. J; YOUNGMAN, S; SARFARAZI, M et al.Journal of medical genetics. 1988, Vol 25, Num 3, pp 191-194, issn 0022-2593Article

The problem of isolated cases of Huntington's disease in South Wales 1974-1984QUARRELL, O. W. J; TYLER, A; COLE, G et al.Clinical genetics. 1986, Vol 30, Num 5, pp 433-439, issn 0009-9163Article

The personal experience of juvenile Huntington's disease : an interpretative phenomenological analysis of parents' accounts of the primary features of a rare genetic conditionSMITH, J. A; BREWER, H. M; EATOUGH, V et al.Clinical genetics. 2006, Vol 69, Num 6, pp 486-496, issn 0009-9163, 11 p.Article

Exclusion testing for Huntington's disease in pregnancy with a closely linked DNA markerQUARRELL, O. W. J; TYLER, A; UPADHYAYA, M et al.Lancet (British edition). 1987, Num 8545, pp 1281-1283, issn 0140-6736Article

Linkage disequilibrium in Huntington's disease: an improved localisation for the geneSNELL, R. G; LAZAROU, L. P; YOUNGMAN, S et al.Journal of medical genetics. 1989, Vol 26, Num 11, pp 673-675, issn 0022-2593, 3 p.Article

Clinical studies on submicroscopic subtelomeric rearrangements: a checklistDE VRIES, B. B. A; WHITE, S. M; TRAINER, A. H et al.Journal of medical genetics. 2001, Vol 38, Num 3, pp 145-150, issn 0022-2593Article

ATRX encodes a novel member of the SNF2 family of proteins : mutations point to a common mechanism underlying the ATR-X syndromePICKETTS, D. J; HIGGS, D. R; BACHOO, S et al.Human molecular genetics (Print). 1996, Vol 5, Num 12, pp 1899-1907, issn 0964-6906Article

Paternal origin of the chromosomal deletion resulting in Wolf-Hirschhorn syndromeQUARRELL, O. W. J; SNELL, R. G; CURTIS, M. A et al.Journal of medical genetics. 1991, Vol 28, Num 4, pp 256-259, issn 0022-2593Article

Detecting deletions in the critical region for lisencephaly on 17p13.3 using fluorescent in situ hybridisation and a PCR assay identifying a dinucleotide repeat polymorphismPILZ, D. T; DALTON, A; LONG, A et al.Journal of medical genetics. 1995, Vol 32, Num 4, pp 275-278, issn 0022-2593Article

Genetic linkage analysis in hereditary non-polyposis colon cancer syndromeFROGGATT, N. J; KOCH, J; MAHER, E. R et al.Journal of medical genetics. 1995, Vol 32, Num 5, pp 352-357, issn 0022-2593Article

Insurance and the presymptomatic diagnosis of delayed-onset disease. ReplyQUARRELL, O. W. J; BLOCH, M; HAYDEN, M. R et al.JAMA, the journal of the American Medical Association. 1989, Vol 262, Num 17, pp 2384-2385, issn 0098-7484, 2 p.Article