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Results of search for 'au:"FORREST, S"', page 6 of 9
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Authors
Cotton, R G
Cross, G S
Dahl, H H
Davies, K E
Delatycki, M B
Dianzani, I
Fitzpatrick, E
Forrest, S
Forrest, S M
Forrest, S R
Gardner, R J
Gittleson, Forrest S
Kenwrick, S J
Knight, M
Nasioulas, S
Roth, Forrest S
Smith, T J
Speer, A
Taylor, André D
Williamson, R
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Adolescent
Adult
Base Sequence
Child
DNA
Exons
Female
Humans
Male
Middle Aged
Molecular Sequence Data
Muscular Dystrophies
Mutation
Pedigree
Phenotype
Polymerase Chain Reaction
X Chromosome
diagnosis
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101.
Preferential deletion of exons in Duchenne and Becker muscular dystrophies.
[electronic resource]
by
Forrest, S M
Cross, G S
Speer, A
Gardner-Medwin, D
Burn, J
Davies, K E
Producer:
19871118
In:
Nature
vol. 329
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102.
Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies.
[electronic resource]
by
Forrest, S M
Cross, G S
Flint, T
Speer, A
Robson, K J
Davies, K E
Producer:
19881011
In:
Genomics
vol. 2
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103.
Kallmann syndrome gene (KAL-X) is not mutated in schizophrenia.
[electronic resource]
by
O'Neill, M
Brewer, W
Thornley, C
Copolov, D
Warne, G
Sinclair, A
Forrest, S
Williamson, R
Producer:
19990503
In:
American journal of medical genetics
vol. 88
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104.
High-external-quantum-efficiency organic light-emitting devices.
[electronic resource]
by
Gu, G
Garbuzov, D Z
Burrows, P E
Venkatesh, S
Forrest, S R
Thompson, M E
Producer:
20121002
In:
Optics letters
vol. 22
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105.
Studies of vehicular padding materials.
[electronic resource]
by
Sances, A
Carlin, F H
Herbst, B
Forrest, S
Meyer, S
Khadilkar, A
Friedman, K
Bish, J
Producer:
20011004
In:
Annual proceedings. Association for the Advancement of Automotive Medicine
vol. 44
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106.
Are mutations in MAPT associated with GGT type III?
[electronic resource]
by
Forrest, S L
Halliday, G M
Shepherd, C E
Kwok, J B
Hallupp, M
Kril, J J
Producer:
20210604
In:
Neuropathology and applied neurobiology
vol. 46
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107.
Patterns of exon deletions in Duchenne and Becker muscular dystrophy.
[electronic resource]
by
Read, A P
Mountford, R C
Forrest, S M
Kenwrick, S J
Davies, K E
Harris, R
Producer:
19881108
In:
Human genetics
vol. 80
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108.
Correlating structure and transport behavior in Li
[electronic resource]
by
Gittleson, Forrest S
Ward, Donald K
Jones, Reese E
Zarkesh, Ryan A
Sheth, Tanvi
Foster, Michael E
Publication details:
Physical chemistry chemical physics : PCCP
Aug 2019
In:
Physical chemistry chemical physics : PCCP
vol. 21
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109.
Combined effect of toe out gait and high tibial osteotomy on knee adduction moment in patients with varus knee deformity.
[electronic resource]
by
Whelton, C
Thomas, A
Elson, D W
Metcalfe, A
Forrest, S
Wilson, C
Holt, C
Whatling, G
Producer:
20170905
In:
Clinical biomechanics (Bristol, Avon)
vol. 43
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110.
DNA amplification of a further exon of Duchenne muscular dystrophy locus increase possibilities for deletion screening.
[electronic resource]
by
Speer, A
Rosenthal, A
Billwitz, H
Hanke, R
Forrest, S M
Love, D
Davies, K E
Coutelle, C
Producer:
19890825
In:
Nucleic acids research
vol. 17
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111.
Molecular analysis of Duchenne and Becker muscular dystrophies.
[electronic resource]
by
Love, D R
Forrest, S M
Smith, T J
England, S
Flint, T
Davies, K E
Speer, A
Producer:
19900208
In:
British medical bulletin
vol. 45
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112.
Ultrathin Nanotube/Nanowire Electrodes by Spin-Spray Layer-by-Layer Assembly: A Concept for Transparent Energy Storage.
[electronic resource]
by
Gittleson, Forrest S
Hwang, Daniel
Ryu, Won-Hee
Hashmi, Sara M
Hwang, Jonathan
Goh, Tenghooi
Taylor, André D
Producer:
20160126
In:
ACS nano
vol. 9
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113.
Isolation of a conserved sequence deleted in Duchenne muscular dystrophy patients.
[electronic resource]
by
Smith, T J
Wilson, L
Kenwrick, S J
Forrest, S M
Speer, A
Coutelle, C
Davies, K E
Producer:
19870501
In:
Nucleic acids research
vol. 15
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114.
Identifying genes predisposing to atopic eczema.
[electronic resource]
by
Forrest, S
Dunn, K
Elliott, K
Fitzpatrick, E
Fullerton, J
McCarthy, M
Brown, J
Hill, D
Williamson, R
Producer:
19991222
In:
The Journal of allergy and clinical immunology
vol. 104
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115.
Spinocerebellar ataxia type 20 is genetically distinct from spinocerebellar ataxia type 5.
[electronic resource]
by
Lorenzo, D N
Forrest, S M
Ikeda, Y
Dick, K A
Ranum, L P W
Knight, M A
Producer:
20070108
In:
Neurology
vol. 67
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116.
Regioselectivity of the insertion reactions of some aromatic diazo compound complexes with cyclomaltoheptaose.
[electronic resource]
by
Smith, S H
Forrest, S M
Williams, D C
Cabell, M F
Acquavella, M F
Abelt, C J
Producer:
19921123
In:
Carbohydrate research
vol. 230
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117.
Direct evidence that mitochondrial iron accumulation occurs in Friedreich ataxia.
[electronic resource]
by
Delatycki, M B
Camakaris, J
Brooks, H
Evans-Whipp, T
Thorburn, D R
Williamson, R
Forrest, S M
Producer:
19990525
In:
Annals of neurology
vol. 45
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118.
Molecular analysis and diagnosis of Duchenne muscular dystrophy.
[electronic resource]
by
Forrest, S M
Smith, T J
Cross, G S
Kenwrick, S J
England, S
Flint, T
Davies, K E
Producer:
19880908
In:
Journal of the Royal College of Physicians of London
vol. 22
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119.
Familial adenomatous polyposis in a 5 year old child: a clinical, pathological, and molecular genetic study.
[electronic resource]
by
Distante, S
Nasioulas, S
Somers, G R
Cameron, D J
Young, M A
Forrest, S M
Gardner, R J
Producer:
19970512
In:
Journal of medical genetics
vol. 33
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120.
Profuse familial adenomatous polyposis with an adenomatous polyposis coli exon 3 mutation.
[electronic resource]
by
Nasioulas, S
Jones, I T
St John, D J
Scott, R J
Forrest, S M
McKinlay Gardner, R J
Producer:
20031120
In:
Familial cancer
vol. 1
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