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Results of search for 'au:"Serjeant, B E"', page 2 of 4
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Authors
Ahern, E
Ahern, V
Ashcroft, M T
Beckford, M
Desai, P
Fisher, C
Forbes, M
Grandison, Y
Hayes, R J
Higgs, D R
Kar, B C
Kulozik, A E
Lehmann, H
Mason, K
Mason, K P
Maude, G H
Serjeant, B E
Serjeant, G R
Thomas, P W
Weatherall, D J
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Topics
Adolescent
Adult
Anemia, Sickle Cell
Child
Child, Preschool
Erythrocyte Count
Female
Fetal Hemoglobin
Hemoglobins
Homozygote
Humans
Infant
Jamaica
Male
Middle Aged
Thalassemia
analysis
blood
complications
genetics
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English
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21.
Screening cord bloods for detection of sickle cell disease in Jamaica.
[electronic resource]
by
Serjeant, B E
Forbes, M
Williams, L L
Serjeant, G R
Producer:
19740720
In:
Clinical chemistry
vol. 20
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22.
Fetal haemoglobin and pregnancy in homozygous sickle cell disease.
[electronic resource]
by
Dunn, D T
Poddar, D
Serjeant, B E
Serjeant, G R
Producer:
19890925
In:
British journal of haematology
vol. 72
Online resources:
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23.
Cholelithiasis in Jamaican patients with homozygous sickle cell disease.
[electronic resource]
by
McCall, I W
Desai, P
Serjeant, B E
Serjeant, G R
Producer:
19780321
In:
American journal of hematology
vol. 3
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24.
Microchromatographic quantitation of hemoglobin A levels in phenotypes of sickle cell-beta(+) thalassemia.
[electronic resource]
by
Sweeting, I
Serjeant, B E
Thomas, P W
Serjeant, G R
Producer:
19980206
In:
Journal of chromatography. B, Biomedical sciences and applications
vol. 700
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25.
Comparison of haematological features of the beta0 and beta+ thalassaemia traits in Jamaican Negroes.
[electronic resource]
by
Millard, D P
Mason, K
Serjeant, B E
Serjeant, G R
Producer:
19770902
In:
British journal of haematology
vol. 36
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26.
A simple micromethod for the measurement of fetal haemoglobin.
[electronic resource]
by
Serjeant, B E
Clarke, J M
Desai, P
Serjeant, G R
Producer:
19751212
In:
Journal of clinical pathology
vol. 28
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27.
The clinical features of sickle-cell- thalassaemia in Jamaica.
[electronic resource]
by
Serjeant, G R
Ashcroft, M T
Serjeant, B E
Milner, P F
Producer:
19730904
In:
British journal of haematology
vol. 24
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28.
Hb F Kingston (G gamma 55 [D6] Met leads to Arg).
[electronic resource]
by
Serjeant, G R
Serjeant, B E
Lehmann, H
Dukes, M
Robb, L
Producer:
19830407
In:
FEBS letters
vol. 150
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29.
Jamaican Sbeta+-thalassaemia: mutations and haematology.
[electronic resource]
by
Donaldson, A
Old, J
Fisher, C
Serjeant, B E
Serjeant, G R
Producer:
20000413
In:
British journal of haematology
vol. 108
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30.
HB S-HB Monroe; a sickle cell-beta-thalassemia syndrome.
[electronic resource]
by
Sweeting, I
Serjeant, B E
Serjeant, G R
Kulozik, A E
Vetter, B
Producer:
19980708
In:
Hemoglobin
vol. 22
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31.
Comparison of sickle cell-beta0 thalassaemia with homozygous sickle cell disease.
[electronic resource]
by
Serjeant, G R
Sommereux, A M
Stevenson, M
Mason, K
Serjeant, B E
Producer:
19790516
In:
British journal of haematology
vol. 41
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32.
Comparison of clinical, hematological and molecular findings of Jamaican and Sicilian patients with sickle cell disease.
[electronic resource]
by
Schiliro, G
Russo Mancuso, G
Kulozik, A E
Serjeant, B E
Serjeant, G R
Producer:
19910517
In:
Haematologica
vol. 75 Suppl 5
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33.
Heights and weights of West Indian children with the sickle cell trait.
[electronic resource]
by
Ashcroft, M T
Desai, P
Grell, G A
Serjeant, B E
Serjeant, G R
Producer:
19781025
In:
Archives of disease in childhood
vol. 53
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34.
Sickle cell-beta+ thalassaemia in Orissa State, India.
[electronic resource]
by
Kulozik, A E
Bail, S
Kar, B C
Serjeant, B E
Serjeant, G E
Producer:
19910422
In:
British journal of haematology
vol. 77
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35.
Plasma proteins in children with trichuris dysentery syndrome.
[electronic resource]
by
Cooper, E S
Ramdath, D D
Whyte-Alleng, C
Howell, S
Serjeant, B E
Producer:
19970529
In:
Journal of clinical pathology
vol. 50
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36.
Haematological response to parvovirus B19 infection in homozygous sickle-cell disease.
[electronic resource]
by
Serjeant, B E
Hambleton, I R
Kerr, S
Kilty, C G
Serjeant, G R
Producer:
20011219
In:
Lancet (London, England)
vol. 358
Online resources:
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37.
Sickle cell-Hb Lepore Boston syndrome. Uncommon differential diagnosis to homozygous sickle cell disease.
[electronic resource]
by
Stevens, M C
Lehmann, H
Mason, K P
Serjeant, B E
Serjeant, G R
Producer:
19820326
In:
American journal of diseases of children (1960)
vol. 136
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38.
Coagulation changes during the steady state in homozygous sickle-cell disease in Jamaica.
[electronic resource]
by
Leslie, J
Langler, D
Serjeant, G R
Serjeant, B E
Desai, P
Gordon, Y B
Producer:
19760301
In:
British journal of haematology
vol. 30
Online resources:
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39.
The haematology of steady state homozygous sickle cell disease: frequency distributions, variation with age and sex, longitudinal observations.
[electronic resource]
by
Hayes, R J
Beckford, M
Grandison, Y
Mason, K
Serjeant, B E
Serjeant, G R
Producer:
19850328
In:
British journal of haematology
vol. 59
Online resources:
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40.
Interaction of the alpha alpha alpha globin gene haplotype and sickle haemoglobin.
[electronic resource]
by
Higgs, D R
Clegg, J B
Weatherall, D J
Serjeant, B E
Serjeant, G R
Producer:
19840917
In:
British journal of haematology
vol. 57
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