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Results of search for 'au:"Shrimpton, A E"', page 1 of 2
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Authors
Aldred, M A
Ambrose, J L
Braddock, B R
Bradshaw, C
Brock, D J
Collins, G H
Davis, R L
Dean, J C
Feiglin, D
Holohan, P D
Hoo, J J
Kelly, K F
Kent, P
Lacbawan, F
Langley, C H
Lawrence, D A
McIntosh, I
Robertson, A
Shrimpton, A E
Tanda, S
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Topics
Adult
Animals
Base Sequence
Child, Preschool
Chromosome Mapping
Cystic Fibrosis
Cystic Fibrosis Transmembrane Conductance Regulator
DNA
DNA Transposable Elements
Female
Fetal Diseases
Humans
Male
Mutation
Pedigree
Polymerase Chain Reaction
Pregnancy
diagnosis
genetics
methods
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English
Your search returned 29 results.
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1.
R117H and IVS8-5T cystic fibrosis mutation detection by restriction enzyme digestion.
[electronic resource]
by
Shrimpton, A E
Producer:
20010118
In:
Molecular diagnosis : a journal devoted to the understanding of human disease through the clinical application of molecular biology
vol. 5
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2.
The isolation of polygenic factors controlling bristle score in Drosophila melanogaster. I. Allocation of third chromosome sternopleural bristle effects to chromosome sections.
[electronic resource]
by
Shrimpton, A E
Robertson, A
Producer:
20100628
In:
Genetics
vol. 118
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3.
The Isolation of Polygenic Factors Controlling Bristle Score in Drosophila Melanogaster. II. Distribution of Third Chromosome Bristle Effects within Chromosome Sections.
[electronic resource]
by
Shrimpton, A E
Robertson, A
Producer:
20100628
In:
Genetics
vol. 118
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4.
Non-paternity and prenatal genetic screening.
[electronic resource]
by
Brock, D J
Shrimpton, A E
Producer:
19911206
In:
Lancet (London, England)
vol. 338
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5.
Molecular screening of partners of cystic fibrosis heterozygotes.
[electronic resource]
by
Shrimpton, A E
Brock, D J
Producer:
19920701
In:
Genetic counseling (Geneva, Switzerland)
vol. 3
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6.
Cystic fibrosis mutation frequencies in upstate New York.
[electronic resource]
by
Shrimpton, A E
Borowitz, D
Swender, P
Producer:
19980102
In:
Human mutation
vol. 10
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7.
The incidence of different cystic fibrosis mutations in the Scottish population: effects on prenatal diagnosis and genetic counselling.
[electronic resource]
by
Shrimpton, A E
McIntosh, I
Brock, D J
Producer:
19910906
In:
Journal of medical genetics
vol. 28
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8.
A PCR assay for detecting clonal rearrangement of the TCR-gamma gene.
[electronic resource]
by
Lamberson, C
Hutchison, R E
Shrimpton, A E
Producer:
20010927
In:
Molecular diagnosis : a journal devoted to the understanding of human disease through the clinical application of molecular biology
vol. 6
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9.
Transposable element-induced response to artificial selection in Drosophila melanogaster: molecular analysis of selection lines.
[electronic resource]
by
Shrimpton, A E
Mackay, T F
Brown, A J
Producer:
19901018
In:
Genetics
vol. 125
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10.
Narrowing the map of a gene (MRXS9) for X-linked mental retardation, microcephaly, and variably short stature at Xq12-q21.31.
[electronic resource]
by
Shrimpton, A E
Braddock, B R
Hoo, J J
Producer:
20000524
In:
American journal of medical genetics
vol. 92
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11.
Mapping of a gene (MRXS9) for X-linked mental retardation, microcephaly, and variably short stature to Xq12-q21.31.
[electronic resource]
by
Shrimpton, A E
Daly, K M
Hoo, J J
Producer:
19990624
In:
American journal of medical genetics
vol. 84
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12.
OM Mutations in DROSOPHILA ANANASSAE Are Linked to Insertions of a Transposable Element.
[electronic resource]
by
Shrimpton, A E
Montgomery, E A
Langley, C H
Producer:
20100628
In:
Genetics
vol. 114
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13.
Presymptomatic testing for autosomal dominant spinocerebellar ataxia type 1.
[electronic resource]
by
Shrimpton, A E
Davidson, R
MacDonald, N
Brock, D J
Producer:
19931025
In:
Journal of medical genetics
vol. 30
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14.
Cystic fibrosis: the new genetics.
[electronic resource]
by
Brock, D J
Shrimpton, A E
Jones, C
McIntosh, I
Producer:
19910626
In:
Journal of the Royal Society of Medicine
vol. 84 Suppl 18
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15.
Screening for carriers of cystic fibrosis.
[electronic resource]
by
Dean, J C
Kelly, K F
Miedzybrodzka, Z
Shrimpton, A E
Producer:
19910314
In:
BMJ (Clinical research ed.)
vol. 302
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16.
Analysis of the Om(1D) locus in Drosophila ananassae.
[electronic resource]
by
Tanda, S
Shrimpton, A E
Hinton, C W
Langley, C H
Producer:
19900208
In:
Genetics
vol. 123
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17.
Syndrome of short stature, widow's peak, ptosis, posteriorly angulated ears, and joint problems: exclusion of the Aarskog (FGD1) gene as a candidate gene.
[electronic resource]
by
LaDine, B J
Simmons, J A
Shrimpton, A E
Hoo, J J
Producer:
20010426
In:
American journal of medical genetics
vol. 99
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18.
Molecular delineation of deletions on 2q37.3 in three cases with an Albright hereditary osteodystrophy-like phenotype.
[electronic resource]
by
Shrimpton, A E
Braddock, B R
Thomson, L L
Stein, C K
Hoo, J J
Producer:
20051114
In:
Clinical genetics
vol. 66
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19.
Naturally occurring variation in the restriction map of the amy region of Drosophila melanogaster.
[electronic resource]
by
Langley, C H
Shrimpton, A E
Yamazaki, T
Miyashita, N
Matsuo, Y
Aquadro, C F
Producer:
20100628
In:
Genetics
vol. 119
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20.
Inheritance of osteosarcoma and Paget's disease of bone: a familial loss of heterozygosity study.
[electronic resource]
by
McNairn, J D
Damron, T A
Landas, S K
Ambrose, J L
Shrimpton, A E
Producer:
20020116
In:
The Journal of molecular diagnostics : JMD
vol. 3
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