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Results of search for 'au:"CONNOR, J M"', page 4 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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Chromosome Mapping
DNA
Down Syndrome
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analysis
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61.
Linkage study of 15 North American families with tuberous sclerosis (TSC)
[electronic resource]
by
Sampson, J R
Connor, J M
Yates, J R
Producer:
19900813
In:
Genomics
vol. 7
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62.
Histocompatibility antigens in patients with ectopic ossification due to fibrodysplasia ossificans progressiva.
[electronic resource]
by
Connor, J M
Woodrow, J C
Evans, D A
Producer:
19830119
In:
Annals of the rheumatic diseases
vol. 41
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63.
Cardiopulmonary function in fibrodysplasia ossificans progressiva.
[electronic resource]
by
Connor, J M
Evans, C C
Evans, D A
Producer:
19820225
In:
Thorax
vol. 36
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64.
Characterisation of inherited and sporadic mutations in neurofibromatosis type-1.
[electronic resource]
by
Purandare, S M
Lanyon, W G
Connor, J M
Producer:
19950105
In:
Human molecular genetics
vol. 3
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65.
Second-trimester unconjugated oestriol levels in maternal serum from chromosomally abnormal pregnancies using an optimized assay.
[electronic resource]
by
Crossley, J A
Aitken, D A
Connor, J M
Producer:
19930707
In:
Prenatal diagnosis
vol. 13
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66.
Evidence for genetic heterogeneity in hereditary hydronephrosis caused by pelvi-ureteric junction obstruction, with one locus assigned to chromosome 6p.
[electronic resource]
by
Izquierdo, L
Porteous, M
Paramo, P G
Connor, J M
Producer:
19920825
In:
Human genetics
vol. 89
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67.
Free beta-hCG as first-trimester marker for fetal trisomy.
[electronic resource]
by
Spencer, K
Macri, J N
Aitken, D A
Connor, J M
Producer:
19920713
In:
Lancet (London, England)
vol. 339
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68.
Monozygous twins concordant for duodenojejunal villous atrophy and dermatitis herpetiformis.
[electronic resource]
by
Green, S T
Natarajan, S
Connor, J M
Forrest, J A
Producer:
19860925
In:
Gut
vol. 27
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69.
CDKN2A germline mutations in U.K. patients with familial melanoma and multiple primary melanomas.
[electronic resource]
by
MacKie, R M
Andrew, N
Lanyon, W G
Connor, J M
Producer:
19980819
In:
The Journal of investigative dermatology
vol. 111
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70.
Insulin-dependent diabetes mellitus and prenatal screening results: current experience from a regional screening programme.
[electronic resource]
by
Crossley, J A
Berry, E
Aitken, D A
Connor, J M
Producer:
19970306
In:
Prenatal diagnosis
vol. 16
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71.
Isolation of chromosome-21-specific DNA probes and their use in the analysis of nondisjunction in Down syndrome.
[electronic resource]
by
Galt, J
Boyd, E
Connor, J M
Ferguson-Smith, M A
Producer:
19890306
In:
Human genetics
vol. 81
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72.
Concordant monozygotic twins with bilateral renal agenesis.
[electronic resource]
by
Yates, J R
Mortimer, G
Connor, J M
Duke, J E
Producer:
19840319
In:
Journal of medical genetics
vol. 21
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73.
Impact of a regional screening programme using maternal serum alpha fetoprotein (AFP) and human chorionic gonadotrophin (hCG) on the birth incidence of Down's syndrome in the west of Scotland.
[electronic resource]
by
Crossley, J A
Aitken, D A
Berry, E
Connor, J M
Producer:
19961018
In:
Journal of medical screening
vol. 1
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74.
Placental synthesis of oestriol in Down's syndrome pregnancies.
[electronic resource]
by
Newby, D
Aitken, D A
Howatson, A G
Connor, J M
Producer:
20000525
In:
Placenta
vol. 21
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75.
Characterisation of a novel splice donor mutation affecting position +1 in intron 18 of the NF-1 gene.
[electronic resource]
by
Purandare, S M
Lanyon, W G
Arngrimsson, R
Connor, J M
Producer:
19950911
In:
Human molecular genetics
vol. 4
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76.
Detection of seven point mutations in the porphobilinogen deaminase gene in patients with acute intermittent porphyria, by direct sequencing of in vitro amplified cDNA.
[electronic resource]
by
Mgone, C S
Lanyon, W G
Moore, M R
Connor, J M
Producer:
19921201
In:
Human genetics
vol. 90
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77.
Regional assignment of the human C1-inhibitor gene to 11q11-q13.1.
[electronic resource]
by
Theriault, A
Whaley, K
McPhaden, A R
Boyd, E
Connor, J M
Producer:
19900518
In:
Human genetics
vol. 84
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78.
Genetic localisation of MRX27 to Xq24-26 defines another discrete gene for non-specific X-linked mental retardation.
[electronic resource]
by
Gedeon, A K
Glass, I A
Connor, J M
Mulley, J C
Producer:
19961120
In:
American journal of medical genetics
vol. 64
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79.
The psychosocial sequelae of a second trimester termination of pregnancy for fetal abnormality over a two year period.
[electronic resource]
by
White-Van Mourik, M C
Connor, J M
Ferguson-Smith, M A
Producer:
19931217
In:
Birth defects original article series
vol. 28
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80.
Mucosal neuroma syndrome--a phenotype for malignancy.
[electronic resource]
by
White, M P
Goel, K M
Connor, J M
Coutts, N A
Producer:
19851118
In:
Archives of disease in childhood
vol. 60
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