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Results of search for 'au:"Ferguson-Smith, M E"', page 1 of 2
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Authors
Affara, N A
Aitken, D A
Alexander, J
Alexander, J L
Batstone, P
Besley, G T
Boyd, E
Briggs, H
Carr, C
Carter, N
Carter, N P
Carty, M J
Ferguson-Smith, M A
Ferguson-Smith, M E
Gilmore, D H
Gompertz, D
Goodey, P A
Russell, G
Thom, H
Tolmie, J L
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Topics
Adult
Amniocentesis
Amniotic Fluid
Cells, Cultured
Chromosome Aberrations
Chromosome Disorders
Down Syndrome
Female
Humans
In Situ Hybridization, Fluorescence
Infant, Newborn
Karyotyping
Male
Mosaicism
Pregnancy
Prenatal Diagnosis
cytology
diagnosis
genetics
methods
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English
Your search returned 22 results.
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1.
Ethical and legal implications in IVF and prenatal diagnosis in the U.K.
[electronic resource]
by
Ferguson-Smith, M E
Producer:
19920220
In:
Prenatal diagnosis
vol. 11
Online resources:
Available from publisher's website
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2.
Problems of prenatal diagnosis.
[electronic resource]
by
Ferguson-Smith, M A
Ferguson-Smith, M E
Producer:
19840329
In:
Proceedings of the annual symposium of the Eugenics Society
vol. 19
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3.
Screening for fetal chromosome aberrations in early pregnancy.
[electronic resource]
by
Ferguson-Smith, M A
Ferguson-Smith, M E
Producer:
19761203
In:
Journal of clinical pathology. Supplement (Royal College of Pathologists)
vol. 10
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4.
Normal development in two six-year-old boys born after prenatal diagnosis of trisomy 20 mosaicism.
[electronic resource]
by
Tolmie, J L
Ferguson-Smith, M E
Gilmore, D
Ferguson-Smith, M A
Producer:
19871222
In:
Prenatal diagnosis
vol. 7
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5.
Chromosome analysis before birth and its value in genetic counselling.
[electronic resource]
by
Ferguson-Smith, M E
Ferguson-Smith, M A
Nevin, N C
Stone, M
Producer:
19711208
In:
British medical journal
vol. 4
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6.
The sites and relative frequencies of secondary constrictions in human somatic chromosomes.
[electronic resource]
by
FERGUSON-SMITH, M A
FERGUSON-SMITH, M E
ELLIS, P M
DICKSON, M
Producer:
19981101
In:
Cytogenetics
vol. 1
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7.
Aneuploidy and cystic hygroma detectable by ultrasound.
[electronic resource]
by
Redford, D H
McNay, M B
Ferguson-Smith, M E
Jamieson, M E
Producer:
19850122
In:
Prenatal diagnosis
vol. 4
Online resources:
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8.
Prenatal screening for congenital abnormalities in the West of Scotland.
[electronic resource]
by
Ferguson-Smith, M A
Ferguson-Smith, M E
Vince, J D
Robinson, H P
Producer:
19760901
In:
Health bulletin
vol. 34
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9.
First trimester diagnosis of Gaucher disease in a fetus with trisomy 21.
[electronic resource]
by
Besley, G T
Ferguson-Smith, M E
Frew, C
Morris, A
Gilmore, D H
Producer:
19890215
In:
Prenatal diagnosis
vol. 8
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10.
Down's syndrome due to maternal mosaicism, and the value of antenatal diagnosis.
[electronic resource]
by
Timson, J
Harris, R
Gadd, R L
Ferguson-Smith, M E
Ferguson-Smith, M A
Producer:
19710406
In:
Lancet (London, England)
vol. 1
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11.
Prenatal diagnosis of a double bisatellited marker with an unusual copy number ratio.
[electronic resource]
by
Waters, J J
Ferguson-Smith, M E
Carter, N
Alexander, J L
Hodgson, S V
Producer:
19910228
In:
Prenatal diagnosis
vol. 10
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12.
Study of X chromosome abnormality in XX males using bivariate flow karyotype analysis and flow sorted dot blots.
[electronic resource]
by
Carter, N P
Ferguson-Smith, M E
Affara, N A
Briggs, H
Ferguson-Smith, M A
Producer:
19900412
In:
Cytometry
vol. 11
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13.
Prenatal detection of trisomy 21 in uncultured amniocytes by fluorescence in situ hybridization: a prospective study.
[electronic resource]
by
Spathas, D H
Divane, A
Maniatis, G M
Ferguson-Smith, M E
Ferguson-Smith, M A
Producer:
19950406
In:
Prenatal diagnosis
vol. 14
Online resources:
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14.
Siblings with chromosome mosaicism, microcephaly, and growth retardation: the phenotypic expression of a human mitotic mutant?
[electronic resource]
by
Tolmie, J L
Boyd, E
Batstone, P
Ferguson-Smith, M E
al Roomi, L
Connor, J M
Producer:
19881108
In:
Human genetics
vol. 80
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15.
Isochromosome for long arm of Y chromosome in patient with Turner's syndrome and sex chromosome mosaicism (45,X-46,XYqi).
[electronic resource]
by
Ferguson-Smith, M A
Boyd, E
Ferguson-Smith, M E
Pritchard, J G
Yusuf, A F
Gray, B
Producer:
19700305
In:
Journal of medical genetics
vol. 6
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16.
Early prenatal investigation of a pregnancy at risk of adenosine deaminase deficiency using chorionic villi.
[electronic resource]
by
Aitken, D A
Gilmore, D H
Frew, C A
Ferguson-Smith, M E
Carty, M J
Chatfield, W R
Producer:
19860402
In:
Journal of medical genetics
vol. 23
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17.
Analysis of chromosome 21 copy number in uncultured amniocytes by fluorescence in situ hybridization using a cosmid contig.
[electronic resource]
by
Zheng, Y L
Ferguson-Smith, M A
Warner, J P
Ferguson-Smith, M E
Sargent, C A
Carter, N P
Producer:
19930305
In:
Prenatal diagnosis
vol. 12
Online resources:
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18.
Antenatal diagnosis of propianicacidaemia.
[electronic resource]
by
Gompertz, D
Goodey, P A
Thom, H
Russell, G
MacLean, M V
Ferguson-Smith, M E
Ferguson-Smith, M A
Producer:
19730621
In:
Lancet (London, England)
vol. 1
Online resources:
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19.
A male with trisomy 9 mosaicism and maternal uniparental disomy for chromosome 9 in the euploid cell line.
[electronic resource]
by
Willatt, L R
Davison, B C
Goudie, D
Alexander, J
Dyson, H M
Jenks, P E
Ferguson-Smith, M E
Producer:
19921127
In:
Journal of medical genetics
vol. 29
Online resources:
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20.
Second-trimester maternal serum screening using alpha-fetoprotein, human chorionic gonadotrophin, and unconjugated oestriol: experience of a regional programme.
[electronic resource]
by
Goodburn, S F
Yates, J R
Raggatt, P R
Carr, C
Ferguson-Smith, M E
Kershaw, A J
Milton, P J
Ferguson-Smith, M A
Producer:
19941010
In:
Prenatal diagnosis
vol. 14
Online resources:
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