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Diagnostic Histopathology
|
July 1, 1983
Lectin binding to normal and malignant breast tissue
A Leathem, I Dokal, N Atkins
Journal of Medical Genetics
|
July 1, 1993
Dyskeratosis congenita: three additional families show linkage to a locus in Xq28
R Arngrimsson, I Dokal, L Luzzatto, et al.
Human Genetics
|
December 1, 1991
Detection of hereditary haemochromatosis in an HLA-identical pedigree showing discordance between HLA class I genes and the disease locus
I Dokal, D Lord, D Rhodes, et al.
British Journal of Haematology
|
September 30, 1998
Chromosomal breakage analysis in dyskeratosis congenita peripheral blood lymphocytes
S Coulthard, A Chase, J Pickard, et al.
British Journal of Haematology
|
November 14, 1997
Adult onset of acute myeloid leukaemia (M6) in patients with Shwachman-Diamond syndrome
I Dokal, S Rule, F Chen, et al.
Blood
|
October 6, 1997
Skewed X-inactivation in carriers of X-linked dyskeratosis congenita
T J Vulliamy, S W Knight, I Dokal, et al.
Blood Cells, Molecules & Diseases
|
March 22, 2001
Very short telomeres in the peripheral blood of patients with X-linked and autosomal dyskeratosis congenita
T J Vulliamy, S W Knight, P J Mason, et al.
Blood
|
December 15, 1992
Dyskeratosis congenita fibroblasts are abnormal and have unbalanced chromosomal rearrangements
I Dokal, J Bungey, P Williamson, et al.
British Journal of Haematology
|
January 1, 1989
Allogeneic bone marrow transplantation for primary myelofibrosis
I Dokal, L Jones, M Deenmamode, et al.
European Journal of Haematology
|
January 1, 1989
Development of polycythaemia vera in a patient with myelofibrosis
I Dokal, A Pagliuca, M Deenmamode, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 55) with videos related to
Sort By:
Page
of 6
Diagnostic Histopathology
|
July 1, 1983
Lectin binding to normal and malignant breast tissue
A Leathem, I Dokal, N Atkins
Journal of Medical Genetics
|
July 1, 1993
Dyskeratosis congenita: three additional families show linkage to a locus in Xq28
R Arngrimsson, I Dokal, L Luzzatto, et al.
Human Genetics
|
December 1, 1991
Detection of hereditary haemochromatosis in an HLA-identical pedigree showing discordance between HLA class I genes and the disease locus
I Dokal, D Lord, D Rhodes, et al.
British Journal of Haematology
|
September 30, 1998
Chromosomal breakage analysis in dyskeratosis congenita peripheral blood lymphocytes
S Coulthard, A Chase, J Pickard, et al.
British Journal of Haematology
|
November 14, 1997
Adult onset of acute myeloid leukaemia (M6) in patients with Shwachman-Diamond syndrome
I Dokal, S Rule, F Chen, et al.
Blood
|
October 6, 1997
Skewed X-inactivation in carriers of X-linked dyskeratosis congenita
T J Vulliamy, S W Knight, I Dokal, et al.
Blood Cells, Molecules & Diseases
|
March 22, 2001
Very short telomeres in the peripheral blood of patients with X-linked and autosomal dyskeratosis congenita
T J Vulliamy, S W Knight, P J Mason, et al.
Blood
|
December 15, 1992
Dyskeratosis congenita fibroblasts are abnormal and have unbalanced chromosomal rearrangements
I Dokal, J Bungey, P Williamson, et al.
British Journal of Haematology
|
January 1, 1989
Allogeneic bone marrow transplantation for primary myelofibrosis
I Dokal, L Jones, M Deenmamode, et al.
European Journal of Haematology
|
January 1, 1989
Development of polycythaemia vera in a patient with myelofibrosis
I Dokal, A Pagliuca, M Deenmamode, et al.
Page
of 6