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Results: 1-25/32
Authors:
HUTCHESSON ACJ
BUNDEY S
PREECE MA
HALL SK
GREEN A
Citation: Acj. Hutchesson et al., A COMPARISON OF DISEASE AND GENE-FREQUENCIES OF INBORN-ERRORS OF METABOLISM AMONG DIFFERENT ETHNIC-GROUPS IN THE WEST MIDLANDS, UK, Journal of Medical Genetics, 35(5), 1998, pp. 366-370
Authors:
LIU XZ
HOPE C
WALSH J
NEWTON V
KE XM
LIANG CY
XU LR
ZHOU JM
TRUMP D
STEEL KP
BUNDEY S
BROWN SDM
Citation: Xz. Liu et al., MUTATIONS IN THE MYOSIN VIIA GENE CAUSE A WIDE PHENOTYPIC SPECTRUM, INCLUDING ATYPICAL USHER-SYNDROME, American journal of human genetics, 63(3), 1998, pp. 909-912
Authors:
COGAN JD
PRINCE MA
LEKHAKULA S
BUNDEY S
FUTRAKUL A
MCCARTHY EMS
PHILLIPS JA
Citation: Jd. Cogan et al., A NOVEL MECHANISM OF ABERRANT PRE-MESSENGER-RNA SPLICING IN HUMANS, Human molecular genetics, 6(6), 1997, pp. 909-912
Authors:
BUNDEY S
Citation: S. Bundey, FEW PSYCHOLOGICAL CONSEQUENCES OF PRESYMPTOMATIC TESTING FOR HUNTINGTON DISEASE, Lancet, 349(9044), 1997, pp. 4-4
Authors:
MORTON JE
BUNDEY S
WEBB TP
MACDONALD F
RINDL PM
BULLOCK S
Citation: Je. Morton et al., FRAGILE-X-SYNDROME IS LESS COMMON THAN PREVIOUSLY ESTIMATED, Journal of Medical Genetics, 34(1), 1997, pp. 1-5
Authors:
BUNDEY S
HUTCHESSON A
DAY A
LANCASHIRE R
Citation: S. Bundey et al., ARE GENETIC-DISEASES LESS COMMON THAN EXPECTED IN AFRO-CARIBBEAN, Journal of Medical Genetics, 34, 1997, pp. 14-14
Authors:
BUNDEY S
Citation: S. Bundey, PREVALENCE AND TYPE OF CEREBRAL-PALSY, Developmental Medicine and Child Neurology, 39(8), 1997, pp. 568-568
Authors:
MITCHELL S
BUNDEY S
Citation: S. Mitchell et S. Bundey, SYMMETRY OF NEUROLOGICAL SIGNS IN PAKISTANI PATIENTS WITH PROBABLE INHERITED SPASTIC CEREBRAL-PALSY, Clinical genetics, 51(1), 1997, pp. 7-14
Authors:
HOPE CI
BUNDEY S
PROOPS D
FIELDER AR
Citation: Ci. Hope et al., USHER-SYNDROME IN THE CITY OF BIRMINGHAM - PREVALENCE AND CLINICAL CLASSIFICATION, British journal of ophthalmology, 81(1), 1997, pp. 46-53
Authors:
TAYLOR TD
HATTORI H
BUNDEY S
MALANDRINI A
VILLANOVA M
FABRIZI GM
MALONE A
LITT M
HAYFLICK SJ
Citation: Td. Taylor et al., EVIDENCE FOR LOCUS HETEROGENEITY IN HALLERVORDEN-SPATZ-SYNDROME, American journal of human genetics, 61(4), 1997, pp. 2357-2357
Authors:
STAVROU P
GOOD PA
BROADHURST EJ
BUNDEY S
FIELDER AR
CREWS SJ
Citation: P. Stavrou et al., ERG AND EOG ABNORMALITIES IN CARRIERS OF X-LINKED RETINITIS-PIGMENTOSA, Eye, 10, 1996, pp. 581-589
Authors:
ROBERTS A
CULLEN R
BUNDEY S
Citation: A. Roberts et al., THE REPRESENTATION OF ETHNIC-MINORITIES AT GENETIC CLINICS IN BIRMINGHAM, Journal of Medical Genetics, 33(1), 1996, pp. 56-58
Authors:
COLLIER DA
BARRETT TG
CURTIS D
MACLEOD A
ARRANZ JM
MAASSEN JA
BUNDEY S
Citation: Da. Collier et al., LINKAGE OF WOLFRAM-SYNDROME TO CHROMOSOME 4P16.1 AND EVIDENCE FOR HETEROGENEITY, American journal of human genetics, 59(4), 1996, pp. 855-863
Authors:
BARRETT TG
POULTON K
BUNDEY S
Citation: Tg. Barrett et al., DIDMOAD SYNDROME - FURTHER-STUDIES AND MUSCLE BIOCHEMISTRY, Journal of inherited metabolic disease, 18(2), 1995, pp. 218-220
Authors:
MORTON JE
RINDL PM
BULLOCK S
BUNDEY S
WEBB T
Citation: Je. Morton et al., FRAGILE-X SYNDROME IS LESS COMMON THAN PREVIOUSLY ESTIMATED, Journal of Medical Genetics, 32(2), 1995, pp. 144-145
Authors:
BARRETT TG
BUNDEY S
Citation: Tg. Barrett et S. Bundey, DIDMOAD SYNDROME - A DEGENERATIVE DILEMMA, Journal of Medical Genetics, 32(2), 1995, pp. 144-144
Authors:
COLLIER DA
BARRETT T
CURTIS D
MACLEOD A
BUNDEY S
Citation: Da. Collier et al., DIDMOAD SYNDROME - CONFIRMATION OF LINKAGE TO CHROMOSOME-4P, EVIDENCEFOR LOCUS HETEROGENEITY AND A PATIENT WITH UNIPARENTAL ISODISOMY FOR CHROMOSOME-49, American journal of human genetics, 57(4), 1995, pp. 1084-1084
Authors:
BUNDEY S
Citation: S. Bundey, CLINICAL AND GENETIC FEATURES OF ATAXIA-TELANGIECTASIA, International journal of radiation biology, 66(6), 1994, pp. 23-29
Authors:
LEE ST
NICHOLLS RD
BUNDEY S
LAXOVA R
MUSARELLA M
SPRITZ RA
Citation: St. Lee et al., MUTATIONS OF THE P-GENE IN OCULOCUTANEOUS ALBINISM, OCULAR ALBINISM, AND PRADER-WILLI-SYNDROME PLUS ALBINISM, The New England journal of medicine, 330(8), 1994, pp. 529-534
Authors:
WATKISS E
BUNDEY S
WEBB T
Citation: E. Watkiss et al., X-INACTIVATION STUDIES IN FEMALE MONOZYGOTIC TWINS, Journal of Medical Genetics, 31(2), 1994, pp. 169-169
Authors:
ALDRED MA
TEAGUE PW
JAY M
BUNDEY S
REDMOND RM
JAY B
BIRD AC
BHATTACHARYA SS
WRIGHT AF
Citation: Ma. Aldred et al., RETINITIS-PIGMENTOSA FAMILIES SHOWING APPARENT X-LINKED INHERITANCE BUT UNLINKED TO THE RP2 OR RP3 LOCI, Journal of Medical Genetics, 31(11), 1994, pp. 848-852
Authors:
WATKISS E
WEBB T
RYSIECKI G
GIRDLER N
HEWETT E
BUNDEY S
Citation: E. Watkiss et al., X-INACTIVATION PATTERNS IN FEMALE MONOZYGOTIC TWINS AND THEIR FAMILIES, Journal of Medical Genetics, 31(10), 1994, pp. 754-757
Authors:
BUNDEY S
HARDY C
VICKERS S
KILPATRICK MW
CORBETT JA
Citation: S. Bundey et al., DUPLICATION OF THE 15Q11-13 REGION IN A PATIENT WITH AUTISM, EPILEPSYAND ATAXIA, Developmental Medicine and Child Neurology, 36(8), 1994, pp. 736-742
Authors:
TEAGUE PW
ALDRED MA
JAY M
DEMPSTER M
HARRISON C
CAROTHERS AD
HARDWICK LJ
EVANS HJ
STRAIN L
BROCK DJH
BUNDEY S
JAY B
BIRD AC
BHATTACHARYA SS
WRIGHT AF
Citation: Pw. Teague et al., HETEROGENEITY ANALYSIS IN 40 X-LINKED RETINITIS-PIGMENTOSA FAMILIES, American journal of human genetics, 55(1), 1994, pp. 105-111
Authors:
CHEN ZY
BATTINELLI EM
FIELDER A
BUNDEY S
SIMS K
BREAKEFIELD XO
CRAIG IW
Citation: Zy. Chen et al., A MUTATION IN THE NORRIE DISEASE GENE (NDP) ASSOCIATED WITH X-LINKED FAMILIAL EXUDATIVE VITREORETINOPATHY, Nature genetics, 5(2), 1993, pp. 180-183