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Results of search for 'au:"Layton, D M"', page 2 of 3
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Authors
Abbas, A
Al-Jafar, Hassan A
Allen, S
Arya, R
Ationu, A
Bailey, N
Bellingham, A J
Buggins, A G
Davies, N P
Green, B N
Humphries, A
Lalloz, M R
Layton, D M
Mufti, G J
Nicolaides, K H
Ofori-Acquah, S F
Pagliuca, A
Percy, M J
Snijders, R J
Wild, B
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Adolescent
Adult
Aged
Anemia, Sickle Cell
Base Sequence
Child
Child, Preschool
Female
Fetal Blood
Genotype
Haplotypes
Humans
Male
Middle Aged
Myelodysplastic Syndromes
Triose-Phosphate Isomerase
analysis
blood
genetics
metabolism
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English
Your search returned 51 results.
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21.
Sweet's syndrome and myelodysplasia.
[electronic resource]
by
Knight, D K
Layton, D M
Mufti, G J
Williams, H
Producer:
19880308
In:
Blut
vol. 56
Online resources:
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22.
Myelodysplastic relapse of de-novo AML: a heterogeneous entity?
[electronic resource]
by
Layton, D M
Ireland, R M
Mufti, G J
Bellingham, A J
Producer:
19880202
In:
Leukemia research
vol. 11
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23.
Safe surgery in sickle cell disease.
[electronic resource]
by
Banerjee, A K
Layton, D M
Rennie, J A
Bellingham, A J
Producer:
19910805
In:
The British journal of surgery
vol. 78
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24.
Fetal plasma interferon gamma concentration in normal pregnancy.
[electronic resource]
by
Abbas, A
Thilaganathan, B
Buggins, A G
Layton, D M
Nicolaides, K H
Producer:
19930622
In:
American journal of obstetrics and gynecology
vol. 168
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25.
Analysis of lymphocyte phenotypes in cord blood from early gestation fetuses.
[electronic resource]
by
Peakman, M
Buggins, A G
Nicolaides, K H
Layton, D M
Vergani, D
Producer:
19921210
In:
Clinical and experimental immunology
vol. 90
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26.
Dominant influence of gamma-globin promoter polymorphisms on fetal haemoglobin expression in sickle cell disease.
[electronic resource]
by
Ofori-Acquah, S F
Lalloz, M R A
Serjeant, G
Layton, D M
Producer:
20041019
In:
Cellular and molecular biology (Noisy-le-Grand, France)
vol. 50
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27.
Fetal plasma tumor necrosis factor concentration in normal pregnancy.
[electronic resource]
by
Abbas, A
Snijders, R J
Buggins, A G
Layton, D M
Nicolaides, K H
Producer:
19940125
In:
Fetal diagnosis and therapy
vol. 8
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28.
Mutation of the human FMS gene (M-CSF receptor) in myelodysplastic syndromes and acute myeloid leukemia.
[electronic resource]
by
Tobal, K
Pagliuca, A
Bhatt, B
Bailey, N
Layton, D M
Mufti, G J
Producer:
19900828
In:
Leukemia
vol. 4
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29.
Prenatal diagnosis of triosephosphate isomerase deficiency.
[electronic resource]
by
Arya, R
Lalloz, M R
Nicolaides, K H
Bellingham, A J
Layton, D M
Producer:
19960718
In:
Blood
vol. 87
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30.
Loss of ras oncogene mutation in a myelodysplastic syndrome after low-dose cytarabine therapy.
[electronic resource]
by
Layton, D M
Mufti, G J
Lyons, J
Janssen, J W
Bartram, C R
Producer:
19880622
In:
The New England journal of medicine
vol. 318
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31.
DNA sequence abnormalities in human glucose 6-phosphate isomerase deficiency.
[electronic resource]
by
Walker, J I
Layton, D M
Bellingham, A J
Morgan, M J
Faik, P
Producer:
19930629
In:
Human molecular genetics
vol. 2
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32.
Disseminated Trichosporon beigelii infection in an immunosuppressed child.
[electronic resource]
by
Higgins, E M
Layton, D M
Arya, R
Salisbury, J
du Vivier, A W
Producer:
19940708
In:
Journal of the Royal Society of Medicine
vol. 87
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33.
Diagnosis of pyrimidine 5'-nucleotidase deficiency suspected from a blood film.
[electronic resource]
by
Al-Jafar, Hassan A
Layton, D M
Robertson, Lynn
Escuredo, Emilia
Bain, Barbara J
Producer:
20140130
In:
American journal of hematology
vol. 88
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34.
Towards enzyme-replacement treatment in triosephosphate isomerase deficiency.
[electronic resource]
by
Ationu, A
Humphries, A
Wild, B
Carr, T
Will, A
Arya, R
Layton, D M
Producer:
19990430
In:
Lancet (London, England)
vol. 353
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35.
Myelofibrosis in primary myelodysplastic syndromes: a clinico-morphological study of 10 cases.
[electronic resource]
by
Pagliuca, A
Layton, D M
Manoharan, A
Gordon, S
Green, P J
Mufti, G J
Producer:
19890619
In:
British journal of haematology
vol. 71
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36.
Two novel mutations in the reduced nicotinamide adenine dinucleotide (NADH)-cytochrome b5 reductase gene of a patient with generalized type, hereditary methemoglobinemia.
[electronic resource]
by
Manabe, J
Arya, R
Sumimoto, H
Yubisui, T
Bellingham, A J
Layton, D M
Fukumaki, Y
Producer:
19961202
In:
Blood
vol. 88
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37.
Quantification of Ggamma- and Agamma-globins by electrospray ionisation mass spectrometry.
[electronic resource]
by
Ofori-Acquah, S F
Green, B N
Wild, B J
Lalloz, M R
Layton, D M
Producer:
20080605
In:
International journal of molecular medicine
vol. 2
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38.
Blood leucocyte count in the human fetus.
[electronic resource]
by
Davies, N P
Buggins, A G
Snijders, R J
Jenkins, E
Layton, D M
Nicolaides, K H
Producer:
19920618
In:
Archives of disease in childhood
vol. 67
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39.
Identification and characterization of the novel FAD-binding lobe G75S mutation in cytochrome b(5) reductase: an aid to determine recessive congenital methemoglobinemia status in an infant.
[electronic resource]
by
Percy, M J
Crowley, L J
Roper, D
Vulliamy, T J
Layton, D M
Barber, M J
Producer:
20060504
In:
Blood cells, molecules & diseases
vol. 36
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40.
Pregnancy outcomes in sickle cell disease: a retrospective cohort study from two tertiary centres in the UK.
[electronic resource]
by
Chase, A R
Sohal, M
Howard, J
Laher, R
McCarthy, A
Layton, D M
Oteng-Ntim, E
Producer:
20160831
In:
Obstetric medicine
vol. 3
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