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Results of search for 'au:"Brock, D J"', page 11 of 13
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Authors
Axton, R A
Barron, L
Bedgood, D
Bloch, K
Brock, D J
Curtis, A
Gilfillan, A
Gosden, C
Hayward, C
Holloway, S
Jones, C T
Liston, W A
McIntosh, I
Mennie, M
Mennie, M E
Scrimgeour, J B
Strain, L
Swingler, R J
Van Heyningen, V
van Heyningen, V
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Topics
Adult
Amniocentesis
Amniotic Fluid
Anencephaly
Cystic Fibrosis
Female
Genetic Carrier Screening
Genetic Testing
Gestational Age
Humans
Male
Pregnancy
Prenatal Diagnosis
Spinal Dysraphism
alpha-Fetoproteins
analysis
diagnosis
enzymology
genetics
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201.
A preliminary trial of couple screening for cystic fibrosis: designing an appropriate information leaflet.
[electronic resource]
by
Livingstone, J
Axton, R A
Mennie, M
Gilfillan, A
Brock, D J
Producer:
19930409
In:
Clinical genetics
vol. 43
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202.
Maternal plasma alpha-fetoprotein and low birthweight: a prospective study throughout pregnancy.
[electronic resource]
by
Brock, D J
Barron, L
Watt, M
Scrimgeour, J B
Keay, A J
Producer:
19820807
In:
British journal of obstetrics and gynaecology
vol. 89
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203.
Screening Alzheimer's disease patients for mutations in the amyloid precursor protein gene.
[electronic resource]
by
Jones, C T
Morris, S
Moffoot, A
St Clair, D
Brock, D J
Producer:
19930730
In:
Molecular and cellular probes
vol. 7
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204.
A single allele from the polymorphic CCG rich sequence immediately 3' to the unstable CAG trinucleotide in the IT15 cDNA shows almost complete disequilibrium with Huntington's disease chromosomes in the Scottish population.
[electronic resource]
by
Barron, L H
Rae, A
Holloway, S
Brock, D J
Warner, J P
Producer:
19940523
In:
Human molecular genetics
vol. 3
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205.
Gene/energy interaction in cystic fibrosis.
[electronic resource]
by
O'Rawe, A
Dodge, J A
Redmond, A O
McIntosh, J
Brock, D J
Producer:
19900406
In:
Lancet (London, England)
vol. 335
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206.
Polymerase chain reaction for detection of the alpha-1-antitrypsin Z allele in chronic liver disease.
[electronic resource]
by
Brind, A M
McIntosh, I
Brock, D J
James, O F
Bassendine, M F
Producer:
19900607
In:
Journal of hepatology
vol. 10
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207.
Two novel mutations and a neutral polymorphism in EGF-like domains of the fibrillin gene (FBN1): SSCP screening of exons 15-21 in Marfan syndrome patients.
[electronic resource]
by
Hayward, C
Rae, A L
Porteous, M E
Logie, L J
Brock, D J
Producer:
19940718
In:
Human molecular genetics
vol. 3
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208.
Prenatal cystic fibrosis carrier screening: factors in a woman's decision to decline testing.
[electronic resource]
by
Mennie, M E
Gilfillan, A
Compton, M E
Liston, W A
Brock, D J
Producer:
19940209
In:
Prenatal diagnosis
vol. 13
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209.
Cu/Zn superoxide dismutase (SOD1) mutations and sporadic amyotrophic lateral sclerosis.
[electronic resource]
by
Jones, C T
Brock, D J
Chancellor, A M
Warlow, C P
Swingler, R J
Producer:
19931118
In:
Lancet (London, England)
vol. 342
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210.
Effect of gestational age on screening for neural-tube defects by maternal plasma-A.F.P. measurement.
[electronic resource]
by
Brock, D J
Scrimgeour, J B
Bolton, A E
Wald, N
Peto, R
Barker, S
Producer:
19751211
In:
Lancet (London, England)
vol. 2
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211.
First-trimester maternal serum biochemical indicators in Down syndrome.
[electronic resource]
by
Brock, D J
Barron, L
Holloway, S
Liston, W A
Hillier, S G
Seppala, M
Producer:
19900813
In:
Prenatal diagnosis
vol. 10
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212.
Enzymes in amniotic fluid: a study of specific activity patterns during pregnancy.
[electronic resource]
by
Sutcliffe, R G
Brock, D J
Robertson, J G
Scrimgeour, J B
Monaghan, J M
Producer:
19730116
In:
The Journal of obstetrics and gynaecology of the British Commonwealth
vol. 79
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213.
HLA-DR and pre-eclampsia in Edinburgh.
[electronic resource]
by
Hayward, C
Gilfillan, A
Livingstone, J
Adam, M
McIntosh, I
Brock, D J
Liston, W A
Producer:
19900718
In:
Lancet (London, England)
vol. 335
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214.
Presymptomatic testing for Huntington's disease. A case complicated by recombination within the D4S10 locus.
[electronic resource]
by
Curtis, A
Millan, F
Holloway, S
Mennie, M
Crosbie, A
Raeburn, J A
Brock, D J
Producer:
19890306
In:
Human genetics
vol. 81
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215.
Expression pattern of two related cystic fibrosis-associated calcium-binding proteins in normal and abnormal tissues.
[electronic resource]
by
Wilkinson, M M
Busuttil, A
Hayward, C
Brock, D J
Dorin, J R
Van Heyningen, V
Producer:
19891106
In:
Journal of cell science
vol. 91 ( Pt 2)
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216.
First trimester diagnosis of hypophosphatasia with a monoclonal antibody to the liver/bone/kidney isoenzyme of alkaline phosphatase.
[electronic resource]
by
Warren, R C
McKenzie, C F
Rodeck, C H
Moscoso, G
Brock, D J
Barron, L
Producer:
19851119
In:
Lancet (London, England)
vol. 2
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217.
The haplotype distribution of the delta F508 mutation in cystic fibrosis families in Scotland.
[electronic resource]
by
McIntosh, I
Curtis, A
Lorenzo, M L
Keston, M
Gilfillan, A J
Morris, G
Brock, D J
Producer:
19901121
In:
Human genetics
vol. 85
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218.
A clue to the basic defect in cystic fibrosis from cloning the CF antigen gene.
[electronic resource]
by
Dorin, J R
Novak, M
Hill, R E
Brock, D J
Secher, D S
van Heyningen, V
Producer:
19870511
In:
Nature
vol. 326
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219.
A study of the Huntington's disease associated trinucleotide repeat in the Scottish population.
[electronic resource]
by
Barron, L H
Warner, J P
Porteous, M
Holloway, S
Simpson, S
Davidson, R
Brock, D J
Producer:
19940418
In:
Journal of medical genetics
vol. 30
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220.
Linkage disequilibrium and recombination make a telomeric site for the Huntington's disease gene unlikely.
[electronic resource]
by
Barron, L
Curtis, A
Shrimpton, A E
Holloway, S
May, H
Snell, R G
Brock, D J
Producer:
19911108
In:
Journal of medical genetics
vol. 28
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