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Results of search for 'au:"Faed, M"', page 2 of 3
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Authors
Batstone, P J
Baxby, K
Beck, J S
Bose, B
Boxer, M
Bridges, A B
Crowder, A M
Delhanty, J D A
Faed, M
Faed, M J
Faed, M J W
Field, M A
Fragouli, E
Frain-Bell, W
Johnson, B E
Lamont, M A
Mills, J A
Mourelatos, D
Robertson, J
West, M R
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Topics
Abnormalities, Multiple
Adolescent
Adult
Aged
Aneuploidy
Cells, Cultured
Chromosome Aberrations
Chromosome Disorders
Female
Humans
Karyotyping
Lymphocytes
Male
Middle Aged
Pedigree
Pregnancy
Sex Chromosome Aberrations
diagnosis
genetics
pathology
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English
Your search returned 49 results.
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21.
A chromosome survey of a hospital for the mentally subnormal.
[electronic resource]
by
Faed, M J
Robertson, J
Field, M A
Mellon, J P
Producer:
19791220
In:
Clinical genetics
vol. 16
Online resources:
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22.
HLA antigens in a Scottish psoriatic population.
[electronic resource]
by
Gunn, I
Leheny, W
Lakshmipathi, T
Lamont, M A
Faed, M
Producer:
19791227
In:
Tissue antigens
vol. 14
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23.
Isodicentric X chromosome in a moderately tall patient with gonadal dysgenesis: lack of effect of functional centromere on inactivation pattern.
[electronic resource]
by
Robertson, J
Faed, M J
Lamont, M A
Crowder, A M
Producer:
19830317
In:
Journal of medical genetics
vol. 19
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24.
Amylo-1,6-glucosidase activity in cultured cells: a deficiency in type III glycogenosis with prenatal studies.
[electronic resource]
by
Besley, G T
Cohen, P T
Faed, M J
Wolstenholme, J
Producer:
19830623
In:
Prenatal diagnosis
vol. 3
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25.
45,X/46,X dic (Y) mosaicism in a phenotypic male.
[electronic resource]
by
Batstone, P J
Faed, M J
Jung, R T
Gosden, J
Producer:
19910410
In:
Archives of disease in childhood
vol. 66
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26.
Deletion of the long arms of chromosome 18 (46,XX,18q-) associated with absence of IgA and hypothyroidism in an adult.
[electronic resource]
by
Faed, M J
Whyte, R
Paterson, C R
McCathie, M
Robertson, J
Producer:
19720718
In:
Journal of medical genetics
vol. 9
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27.
An XYY boy with short stature and a case of Klinefelter's syndrome (XXY) in a family with inversion 9.
[electronic resource]
by
Faed, M J
Lamont, M
Morton, H G
Robertson, J
Smail, P
Producer:
19781227
In:
Clinical genetics
vol. 14
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28.
Pure partial trisomy for long arm of chromosome 9.
[electronic resource]
by
Faed, M
Robertson, J
Brown, S
Smail, P J
Muckhart, R D
Producer:
19760901
In:
Journal of medical genetics
vol. 13
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29.
Incidence of familial Hodgkin's disease.
[electronic resource]
by
Kerzin-Storrar, L
Faed, M J
MacGillivray, J B
Smith, P G
Producer:
19830729
In:
British journal of cancer
vol. 47
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30.
Wiedemann-Beckwith syndrome in one of monozygotic twins.
[electronic resource]
by
Bose, B
Wilkie, R A
Madlom, M
Forsyth, J S
Faed, M J
Producer:
19860307
In:
Archives of disease in childhood
vol. 60
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31.
Persistence of two Y chromosomes through meiotic prophase and metaphase I in an XYY man.
[electronic resource]
by
Speed, R M
Faed, M J
Batstone, P J
Baxby, K
Barnetson, W
Producer:
19911002
In:
Human genetics
vol. 87
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32.
The frequency of constitutional chromosome abnormalities in patients with malignant disease.
[electronic resource]
by
Harnden, D G
Langlands, A O
McBeath, S
O'Riordan, M
Faed, M J
Producer:
19701109
In:
European journal of cancer
vol. 5
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33.
Mechanisms of maternal aneuploidy: FISH analysis of oocytes and polar bodies in patients undergoing assisted conception.
[electronic resource]
by
Mahmood, R
Brierley, C H
Faed, M J
Mills, J A
Delhanty, J D
Producer:
20000821
In:
Human genetics
vol. 106
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34.
Inherited pericentric inversion of chromosome 5: a family with history of neonatal death and a case of the "cri du chat" syndrome.
[electronic resource]
by
Faed, M J
Marrian, V J
Robertson, J
Robson, E B
Cook, P J
Producer:
19730313
In:
Cytogenetics
vol. 11
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35.
Marfan syndrome in a large family: response of family members to a screening programme.
[electronic resource]
by
Bridges, A B
Faed, M
Boxer, M
Gray, J R
Bundy, C
Murray, A
Producer:
19920727
In:
Journal of medical genetics
vol. 29
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36.
Sister chromatid exchanges in lymphocytes of psoriatics after treatment with 8-methoxypsoralen and long wave ultraviolet radiation.
[electronic resource]
by
Mourelatos, D
Faed, M J
Gould, P W
Johnson, B E
Frain-Bell, W
Producer:
19780417
In:
The British journal of dermatology
vol. 97
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37.
Trisomy 21 in transient myeloproliferative disorder.
[electronic resource]
by
Faed, M J
Robertson, J
Todd, A S
Sivakumaran, M
Tarnow-Mordi, W O
Producer:
19901015
In:
Cancer genetics and cytogenetics
vol. 48
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38.
Sister chromatid exchange and chromosome aberration rates in a group of psoriatics before and after a course of PUVA treatment.
[electronic resource]
by
Faed, M J
Williamson, L
Peterson, S
Lakshmipathi, T
Johnson, B E
Frain-Bell, W
Producer:
19810116
In:
The British journal of dermatology
vol. 103
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39.
Features of di George syndrome in a child with 45,XX,-3,-22,+der(3),t(3;22)(p25;q11).
[electronic resource]
by
Faed, M J
Robertson, J
Beck, J S
Cater, J I
Bose, B
Madlom, M M
Producer:
19870716
In:
Journal of medical genetics
vol. 24
Online resources:
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40.
Marfan syndrome affecting four generations of a family without ocular involvement.
[electronic resource]
by
Bridges, A B
Faed, M
Boxer, M
Haining, W M
Pringle, T H
McNeill, G P
Producer:
19911118
In:
Postgraduate medical journal
vol. 67
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