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Results of search for 'au:"Grignoli, C R"'
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Authors
Alberto, F L
Arruda, V R
Carvalho, M H
Costa, F F
Grignoli, C R
Grignoli, C R E
Kimura, E M
Lima, C S
Lorand-Metze, I
Pinheiro, V R P
Saad, S T
Sonati, M F
Wenning, M R
de Melo, M B
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Topics
Acute Disease
Adult
Alleles
Anemia, Aplastic
Aspartic Acid
Brazil
Case-Control Studies
Child
Child, Preschool
Codon
Electrophoresis
Female
Globins
Heterozygote
Humans
Male
Point Mutation
beta-Thalassemia
diagnosis
genetics
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English
Your search returned 4 results.
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1.
Thalassemia intermedia as a result of heterozygosis for beta 0 -thalassemia and alpha alpha alpha anti-3,7 genotype in a Brazilian patient.
[electronic resource]
by
Kimura, E M
Grignoli, C R E
Pinheiro, V R P
Costa, F F
Sonati, M F
Producer:
20031126
In:
Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas
vol. 36
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Available from publisher's website
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2.
beta0-thalassemia resulting from a novel mutation: beta66/u-->stop codon.
[electronic resource]
by
Grignoli, C R
Carvalho, M H
Kimura, E M
Sonati, M F
Arruda, V R
Saad, S T
Costa, F F
Producer:
20001003
In:
European journal of haematology
vol. 64
Online resources:
Available from publisher's website
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No items available.
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3.
Hb Rio Claro [beta34(B16)Val-->Met]: a novel electrophoretically silent variant found in association with Hb Hasharon [alpha47(CE5)Asp-->His] and alpha-thalassemia-2(-alpha3.7).
[electronic resource]
by
Grignoli, C R
Wenning, M R
Sonati, M F
Kimura, E M
Arruda, V R
Saad, S T
Costa, F F
Producer:
19990712
In:
Hemoglobin
vol. 23
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4.
Increased risk for acute myeloid leukaemia in individuals with glutathione S-transferase mu 1 (GSTM1) and theta 1 (GSTT1) gene defects.
[electronic resource]
by
Arruda, V R
Lima, C S
Grignoli, C R
de Melo, M B
Lorand-Metze, I
Alberto, F L
Saad, S T
Costa, F F
Producer:
20010823
In:
European journal of haematology
vol. 66
Online resources:
Available from publisher's website
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No items available.
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