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Results of search for 'au:"CONNOR, J M"', page 6 of 10
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Authors
Aitken, D A
Arngrimsson, R
Beighton, P
Berry, E
Boyd, E
Chu, C E
Connor, J M
Connor, R A
Cooke, A
Crossley, J A
Evans, D A
Ferguson-Smith, M A
Harrap, S B
Lanyon, W G
Lowe, G D
Macri, J N
Moore, M R
Morrison, N
Tolmie, J L
Yates, J R
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Adolescent
Adult
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Base Sequence
Child
Chromosome Mapping
DNA
Down Syndrome
Female
Genetic Linkage
Humans
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Middle Aged
Pedigree
Polymerase Chain Reaction
Pregnancy
analysis
blood
diagnosis
genetics
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Results
101.
Heat-stable and immunoreactive placental alkaline phosphatase in maternal serum from Down's syndrome and trisomy 18 pregnancies.
[electronic resource]
by
Aitken, D A
Syvertsen, B S
Crossley, J A
Berry, E
Connor, J M
Producer:
19970306
In:
Prenatal diagnosis
vol. 16
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102.
The pathophysiology of Down's syndrome pregnancies.
[electronic resource]
by
Newby, D
Aitken, D A
Crossley, J A
Howatson, A G
Connor, J M
Producer:
19970430
In:
Early human development
vol. 47 Suppl
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103.
Mosaic supernumerary ring chromosome 19 identified by comparative genomic hybridisation.
[electronic resource]
by
Ghaffari, S R
Boyd, E
Connor, J M
Jones, A M
Tolmie, J L
Producer:
19990105
In:
Journal of medical genetics
vol. 35
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104.
Placental and maternal serum inhibin-A and activin-A levels in Down's syndrome pregnancies.
[electronic resource]
by
Dalgliesh, G L
Aitken, D A
Lyall, F
Howatson, A G
Connor, J M
Producer:
20010503
In:
Placenta
vol. 22
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105.
Assignment of the human angiotensinogen gene to chromosome 1q42-q43 by nonisotopic in situ hybridization [corrected].
[electronic resource]
by
Isa, M N
Boyd, E
Morrison, N
Harrap, S
Clauser, E
Connor, J M
Producer:
19910325
In:
Genomics
vol. 8
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106.
Detection of an unbalanced translocation (4;14) in a mildly retarded father and son by flow cytometry.
[electronic resource]
by
Cooke, A
Tolmie, J L
Colgan, J M
Greig, C M
Connor, J M
Producer:
19891003
In:
Human genetics
vol. 83
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107.
Assignment of the gene for dyskeratosis congenita to Xq28.
[electronic resource]
by
Connor, J M
Gatherer, D
Gray, F C
Pirrit, L A
Affara, N A
Producer:
19860612
In:
Human genetics
vol. 72
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108.
Tuberous sclerosis: analysis of linkage to red cell and plasma protein markers.
[electronic resource]
by
Connor, J M
Yates, J R
Mann, L
Aitken, D A
Stephenson, J B
Producer:
19870416
In:
Cytogenetics and cell genetics
vol. 44
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109.
Genetic aspects of tuberous sclerosis in the west of Scotland.
[electronic resource]
by
Sampson, J R
Scahill, S J
Stephenson, J B
Mann, L
Connor, J M
Producer:
19890406
In:
Journal of medical genetics
vol. 26
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110.
Analysis of maternal serum alpha-fetoprotein and free beta human chorionic gonadotrophin in the first trimester: implications for Down's syndrome screening.
[electronic resource]
by
Berry, E
Aitken, D A
Crossley, J A
Macri, J N
Connor, J M
Producer:
19951005
In:
Prenatal diagnosis
vol. 15
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111.
Screening for Down's syndrome: changes in marker levels and detection rates between first and second trimesters.
[electronic resource]
by
Berry, E
Aitken, D A
Crossley, J A
Macri, J N
Connor, J M
Producer:
19970904
In:
British journal of obstetrics and gynaecology
vol. 104
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112.
Fibrinogen, factor VII and PAI-1 genotypes and the risk of coronary and peripheral atherosclerosis: Edinburgh Artery Study.
[electronic resource]
by
Lee, A J
Fowkes, F G
Lowe, G D
Connor, J M
Rumley, A
Producer:
19990804
In:
Thrombosis and haemostasis
vol. 81
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113.
Analysis of the origin of Turner's syndrome using polymorphic DNA probes.
[electronic resource]
by
Loughlin, S A
Redha, A
McIver, J
Boyd, E
Carothers, A
Connor, J M
Producer:
19910723
In:
Journal of medical genetics
vol. 28
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114.
Identification of five novel mutations in the porphobilinogen deaminase gene.
[electronic resource]
by
Mgone, C S
Lanyon, W G
Moore, M R
Louie, G V
Connor, J M
Producer:
19941011
In:
Human molecular genetics
vol. 3
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115.
Detection of t(12;21) in childhood acute lymphoblastic leukemia by fluorescence in situ hybridization.
[electronic resource]
by
Spathas, D H
Stewart, J
Singer, I O
Theriault, A
Bovey, M
Connor, J M
Producer:
19990421
In:
Cancer genetics and cytogenetics
vol. 110
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116.
Chromosomal assignment of a glutamic acid transfer RNA (tRNAGlu) gene to 1p36.
[electronic resource]
by
Boyd, E
Theriault, A
Goddard, J P
Kalaitsidaki, M
Spathas, D H
Connor, J M
Producer:
19890306
In:
Human genetics
vol. 81
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117.
Genetic and environmental influences in the development of multiple primary melanoma.
[electronic resource]
by
Burden, A D
Newell, J
Andrew, N
Kavanagh, G
Connor, J M
MacKie, R M
Producer:
19990415
In:
Archives of dermatology
vol. 135
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118.
Confirmation of CHD7 as a cause of CHARGE association identified by mapping a balanced chromosome translocation in affected monozygotic twins.
[electronic resource]
by
Johnson, D
Morrison, N
Grant, L
Turner, T
Fantes, J
Connor, J M
Murday, V
Producer:
20060809
In:
Journal of medical genetics
vol. 43
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119.
Detection of a high mutation frequency in exon 12 of the porphobilinogen deaminase gene in patients with acute intermittent porphyria.
[electronic resource]
by
Mgone, C S
Lanyon, W G
Moore, M R
Louie, G V
Connor, J M
Producer:
19940121
In:
Human genetics
vol. 92
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120.
Detection of mutations in ectopic factor VIII transcripts from nine haemophilia A patients and the correlation with phenotype.
[electronic resource]
by
Bidichandani, S I
Lanyon, W G
Shiach, C R
Lowe, G D
Connor, J M
Producer:
19950627
In:
Human genetics
vol. 95
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