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Results of search for 'au:"CONNOR, J M"', page 5 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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81.
Variation in the levels of pregnancy-specific beta-1-glycoprotein in maternal serum from chromosomally abnormal pregnancies.
[electronic resource]
by
Graham, G W
Crossley, J A
Aitken, D A
Connor, J M
Producer:
19921001
In:
Prenatal diagnosis
vol. 12
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82.
Pycnodysostosis in a Pakistani family: case presentation and review.
[electronic resource]
by
Kerr, A M
Loudon, M M
Goel, K M
Connor, J M
Producer:
19850508
In:
Scottish medical journal
vol. 30
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83.
A novel splice donor mutation affecting position +3 in intron 6 of the factor VIII gene.
[electronic resource]
by
Bidichandani, S I
Shiach, C R
Lanyon, W G
Connor, J M
Producer:
19940927
In:
Human molecular genetics
vol. 3
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84.
Regional chromosomal assignment of genes encoding the alpha and beta subunits of human complement protein C8 to 1p32.
[electronic resource]
by
Theriault, A
Boyd, E
Whaley, K
Sodetz, J M
Connor, J M
Producer:
19920427
In:
Human genetics
vol. 88
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85.
Patient care before and after termination of pregnancy for neural tube defects.
[electronic resource]
by
White-Van Mourik, M C
Connor, J M
Ferguson-Smith, M A
Producer:
19910208
In:
Prenatal diagnosis
vol. 10
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86.
Acute intermittent porphyria: alternative splicing of hydroxymethylbilane synthase mRNA excludes exons 3 and 12.
[electronic resource]
by
Ong, P M
Lanyon, W G
Moore, M R
Connor, J M
Producer:
19980908
In:
Molecular and cellular probes
vol. 12
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87.
Spondylothoracic and spondylocostal dysostosis. Hereditary forms of spinal deformity.
[electronic resource]
by
Roberts, A P
Conner, A N
Tolmie, J L
Connor, J M
Producer:
19880304
In:
The Journal of bone and joint surgery. British volume
vol. 70
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88.
Regional chromosomal assignment of the human platelet phosphofructokinase gene to 10p15.
[electronic resource]
by
Morrison, N
Simpson, C
Fothergill-Gilmore, L
Boyd, E
Connor, J M
Producer:
19920609
In:
Human genetics
vol. 89
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89.
The psychosocial sequelae of a second-trimester termination of pregnancy for fetal abnormality.
[electronic resource]
by
White-van Mourik, M C
Connor, J M
Ferguson-Smith, M A
Producer:
19920619
In:
Prenatal diagnosis
vol. 12
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90.
A practical strategy for detection of major chromosome aneuploidies using ratio-mixing fluorescence in situ hybridization.
[electronic resource]
by
Mohaddes, S M
Boyd, E
Morris, A
Morrison, N
Connor, J M
Producer:
19960920
In:
Molecular and cellular probes
vol. 10
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91.
A novel insertional mutation of a single base in exon 34 of the neurofibromatosis-1 gene.
[electronic resource]
by
Purandare, S M
Davidson, H R
Lanyon, W G
Connor, J M
Producer:
19940407
In:
Human mutation
vol. 3
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92.
Inv dup (15) with mental retardation but few dysmorphic features.
[electronic resource]
by
Gilmore, D H
Boyd, E
McClure, J P
Batstone, P
Connor, J M
Producer:
19840824
In:
Journal of medical genetics
vol. 21
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93.
Is genetic susceptibility for pre-eclampsia and eclampsia associated with implantation failure and fetal demise?
[electronic resource]
by
Arngrimsson, R
Connor, J M
Geirsson, R T
Brennecke, S
Cooper, D W
Producer:
19940719
In:
Lancet (London, England)
vol. 343
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94.
Prediction of liability to orofacial clefting using genetic and craniofacial data from parents.
[electronic resource]
by
Mossey, P A
Arngrimsson, R
McColl, J
Vintiner, G M
Connor, J M
Producer:
19980729
In:
Journal of medical genetics
vol. 35
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95.
Microcephaly: genetic counselling and antenatal diagnosis after the birth of an affected child.
[electronic resource]
by
Tolmie, J L
McNay, M
Stephenson, J B
Doyle, D
Connor, J M
Producer:
19871001
In:
American journal of medical genetics
vol. 27
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96.
Regional chromosomal assignment of the human mineralocorticoid receptor gene to 4q31.1.
[electronic resource]
by
Morrison, N
Harrap, S B
Arriza, J L
Boyd, E
Connor, J M
Producer:
19900801
In:
Human genetics
vol. 85
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97.
Regional chromosomal assignment of the human glucocorticoid receptor gene to 5q31.
[electronic resource]
by
Theriault, A
Boyd, E
Harrap, S B
Hollenberg, S M
Connor, J M
Producer:
19891116
In:
Human genetics
vol. 83
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98.
Identification of chromosome 21 materials using the whole chromosome 21 specific library.
[electronic resource]
by
Isa, M N
Boyd, E
Turner, T L
Tolmie, J
Connor, J M
Producer:
19960626
In:
The Southeast Asian journal of tropical medicine and public health
vol. 26 Suppl 1
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99.
Assignment of the gene encoding the human gonadotropin-releasing hormone receptor to 4q13.2-13.3 by fluorescence in situ hybridization.
[electronic resource]
by
Morrison, N
Sellar, R E
Boyd, E
Eidne, K A
Connor, J M
Producer:
19940719
In:
Human genetics
vol. 93
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100.
Assignment of the gene encoding the human thyrotropin-releasing hormone receptor to 8q23 by fluorescence in situ hybridization.
[electronic resource]
by
Morrison, N
Duthie, S M
Boyd, E
Eidne, K A
Connor, J M
Producer:
19940719
In:
Human genetics
vol. 93
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