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Results of search for 'au:"HUMPHRIES, P"', page 4 of 6
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Authors
Ayuso, C
Bhattacharya, S
Bradley, D G
Bush, R A
Campbell, M
DOBRINER, K
Daiger, S P
Farrar, G J
Gal, A
Humphries, M M
Humphries, P
Jordan, S A
Kenna, P
Kenna, P F
Kiang, A S
Kumar-Singh, R
Lawler, M
McCann, S R
McWilliam, P
Sharp, E M
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Topics
Adult
Animals
Base Sequence
Chromosome Mapping
Female
Genes, Dominant
Genetic Linkage
Genetic Markers
Humans
Male
Mice
Molecular Sequence Data
Mutation
Pedigree
Polymerase Chain Reaction
Polymorphism, Genetic
Retinitis Pigmentosa
Rhodopsin
genetics
methods
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English
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61.
Linkage analysis of X linked retinitis pigmentosa in the Irish population.
[electronic resource]
by
Farrar, G J
Geraghty, M T
Moloney, J M
McConnell, D J
Humphries, P
Producer:
19880616
In:
Journal of medical genetics
vol. 25
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62.
Inhibition of enzyme function by human autoantibodies to an autoantigen pyruvate dehydrogenase E2: different epitope for spontaneous human and induced rabbit autoantibodies.
[electronic resource]
by
Uibo, R
Mackay, I R
Rowley, M
Humphries, P
Armstrong, J M
McNeilage, J
Producer:
19900523
In:
Clinical and experimental immunology
vol. 80
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63.
Frequency of deletion 508 among Irish cystic fibrosis patients.
[electronic resource]
by
De Arce, M A
Mulherin, D
McWilliam, P
Lawler, M
FitzGerald, M X
Humphries, P
Producer:
19901121
In:
Human genetics
vol. 85
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64.
Donor leukemia following allogeneic bone marrow transplantation.
[electronic resource]
by
Mc Cann, S R
Lawler, M
Gardiner, N
O'Riordan, J
Humphries, P
De Arce, M
Producer:
19940506
In:
Leukemia
vol. 8 Suppl 1
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65.
Structure of recombinant plasmids containing synthetic human foetal globin gene sequences.
[electronic resource]
by
Humphries, P
Coggins, L W
Old, R W
Mitchell, G J
Coleclough, C
Paul, J
Producer:
19790124
In:
Molecular & general genetics : MGG
vol. 165
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66.
Mapping of bovine markers CYP21, PRL, and BOLA DRBP1 by genetic linkage analysis in reference pedigrees.
[electronic resource]
by
Creighton, P
Eggen, A
Fries, R
Jordan, S A
Hetzel, J
Cunningham, E P
Humphries, P
Producer:
19921201
In:
Genomics
vol. 14
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67.
Autosomal dominant retinitis pigmentosa: a new multi-allelic marker (D3S621) genetically linked to the disease locus (RP4).
[electronic resource]
by
Kumar-Singh, R
Bradley, D G
Farrar, G J
Lawler, M
Jordan, S A
Humphries, P
Producer:
19910520
In:
Human genetics
vol. 86
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68.
Autosomal dominant retinitis pigmentosa: a new multi-allelic marker (D3S621) genetically linked to the disease locus (RP4).
[electronic resource]
by
Kumar-Singh, R
Bradley, D G
Farrar, G J
Lawler, M
Jordan, S A
Humphries, P
Producer:
19951120
In:
Human genetics
vol. 96
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69.
Novel mutations in the TIGR gene in early and late onset open angle glaucoma.
[electronic resource]
by
Mansergh, F C
Kenna, P F
Ayuso, C
Kiang, A S
Humphries, P
Farrar, G J
Producer:
19980429
In:
Human mutation
vol. 11
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70.
Three novel rhodopsin mutations (C110F, L131P, A164V) in patients with autosomal dominant retinitis pigmentosa.
[electronic resource]
by
Fuchs, S
Kranich, H
Denton, M J
Zrenner, E
Bhattacharya, S S
Humphries, P
Gal, A
Producer:
19950105
In:
Human molecular genetics
vol. 3
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71.
A mutation-independent therapeutic strategem for osteogenesis imperfecta.
[electronic resource]
by
Millington-Ward, S
O'Neill, B
Kiang, A S
Humphries, P
Kenna, P F
Farrar, G J
Producer:
20000214
In:
Antisense & nucleic acid drug development
vol. 9
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72.
The pathophysiology of cigarette smoking and age-related macular degeneration.
[electronic resource]
by
Ni Dhubhghaill, S S
Cahill, M T
Campbell, M
Cassidy, L
Humphries, M M
Humphries, P
Producer:
20110912
In:
Advances in experimental medicine and biology
vol. 664
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73.
Analysis of transcripts homologous to acyl-CoA oxidase and enoyl-CoA hydratase/3-hydroxyacyl-CoA dehydrogenase induced in rat liver by methylclofenapate.
[electronic resource]
by
McQuaid, S
Russell, S E
Withe, S A
Pearson, C M
Elcombe, C R
Humphries, P
Producer:
19871123
In:
Cancer letters
vol. 37
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74.
Further evidence of exclusion of linkage between type II autosomal dominant retinitis pigmentosa (ADRP) and D3S47 on 3q.
[electronic resource]
by
Blanton, S H
Cottingham, A W
Giesenschlag, N
Heckenlively, J R
Humphries, P
Daiger, S P
Producer:
19910509
In:
Genomics
vol. 8
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75.
Exclusion of the involvement of all known retinitis pigmentosa loci in the disease present in a family of Irish origin provides evidence for a sixth autosomal dominant locus (RP8).
[electronic resource]
by
Kumar-Singh, R
Farrar, G J
Mansergh, F
Kenna, P
Bhattacharya, S
Gal, A
Humphries, P
Producer:
19931004
In:
Human molecular genetics
vol. 2
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76.
Polymorphisms and rare sequence variants at the ROM1 locus.
[electronic resource]
by
Bascom, R A
Liu, L
Humphries, P
Fishman, G A
Murray, J C
McInnes, R R
Producer:
19940217
In:
Human molecular genetics
vol. 2
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77.
The EUROGEM map of human chromosome 1.
[electronic resource]
by
Kumar-Singh, R
Wang, H
Carritt, B
Kruse, T A
McCarthy, T V
Vergnaud, G
Humphries, P
Producer:
19950227
In:
European journal of human genetics : EJHG
vol. 2
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78.
Alu polymorphism in the human type I Keratin (KRT14) gene.
[electronic resource]
by
Humphries, M M
Sheils, D M
Jordan, S A
Farrar, G J
Kumar-Singh, R
Humphries, P
Producer:
19930607
In:
Human molecular genetics
vol. 1
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79.
Adenovirus 12 E1A gene detection by polymerase chain reaction in both the normal and coeliac duodenum.
[electronic resource]
by
Lawler, M
Humphries, P
O'Farrelly, C
Hoey, H
Sheils, O
Jeffers, M
O'Briain, D S
Kelleher, D
Producer:
19941208
In:
Gut
vol. 35
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80.
Successful second unrelated donor BMT in a child with juvenile chronic myeloid leukaemia: documentation of chimaerism using the polymerase chain reaction.
[electronic resource]
by
Pamphilon, D H
Cornish, J M
Goodman, S
Ball, L
Lawler, M
McCann, S
Humphries, P
Oakhill, A
Producer:
19930317
In:
Bone marrow transplantation
vol. 11
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