Zobrazeno 1 - 10
of 16
pro vyhledávání: '"J D Hoyer"'
Publikováno v:
Journal of Clinical Pathology. 57:637-640
Aims: To evaluate the technique of multiple displacement amplification (MDA) for whole genome amplification from small volume blood samples before sequencing in a clinical test to identify haemoglobin gene mutations. Methods: Phage φ29 DNA polymeras
Autor:
G E Elder, T R Lappin, A B Horne, V F Fairbanks, R T Jones, P C Winter, B N Green, J D Hoyer, T M Reynolds, D T Shih, D J McCormick, K S Kubik, B J Madden, C G Head, D Harvey, N B Roberts
Publikováno v:
Mayo Clinic Proceedings. 73:321-328
Autor:
A D, Stephens, M, Angastiniotis, E, Baysal, V, Chan, S, Fucharoen, P C, Giordano, J D, Hoyer, A, Mosca, B, Wild
Publikováno v:
International journal of laboratory hematology. 34(1)
Although DNA analysis is needed for characterization of the mutations that cause β-thalassaemia, measurement of the Hb A(2) is essential for the routine identification of people who are carriers of β-thalassaemia. The methods of quantitating Hb A(2
Autor:
A D, Stephens, M, Angastiniotis, E, Baysal, V, Chan, B, Davis, S, Fucharoen, P C, Giordano, J D, Hoyer, A, Mosca, B, Wild
Publikováno v:
International journal of laboratory hematology. 34(1)
Measurement of the Haemoglobin F in red cell haemolysates is important in the diagnosis of δβ thalassaemia, hereditary persistence of fetal haemoglobin (HPFH) and in the diagnosis and management of sickle cell disease. The distribution of Hb F in r
Publikováno v:
American journal of clinical pathology. 113(6)
We identified 24 cases of multiple myeloma with the t(11;14)(q13;q32). In 22 cases, the t(11;14)(q13;q32) was part of a complex karyotype, and in 2 cases it was an isolated abnormality. All patients had clinical and laboratory features consistent wit
Autor:
C A, Hanson, P J, Kurtin, J A, Katzmann, J D, Hoyer, C Y, Li, J M, Hodnefield, C H, Meyers, T M, Habermann, T E, Witzig
Publikováno v:
Blood. 94(11)
This study evaluated the contributing roles of flow cytometric immunophenotyping of blood and bone marrow and immunohistochemical paraffin section staining of bone marrow biopsies in the staging of B-cell malignant lymphoma. Flow immunophenotyping wa
Publikováno v:
Hemoglobin. 23(3)
Publikováno v:
British journal of haematology. 106(2)
A clinicopathologic study was performed on 15 patients with haematological malignancies in which isochromosome 17q [i(17q)] was the sole structural chromosome abnormality identified in bone marrow. The data indicated that an isolated i(17q) is associ
Publikováno v:
British journal of haematology. 104(4)
B-cell chronic lymphocytic leukaemia is an indolent disease characterized by the insidious accumulation of small mature-appearing lymphocytes in the peripheral blood, bone marrow and lymphoid tissues. Direct symptomatic invasion of the central nervou
Autor:
G E, Elder, T R, Lappin, A B, Horne, V F, Fairbanks, R T, Jones, P C, Winter, B N, Green, J D, Hoyer, T M, Reynolds, D T, Shih, D J, McCormick, K S, Kubik, B J, Madden, C G, Head, D, Harvey, N B, Roberts
Publikováno v:
Mayo Clinic proceedings. 73(4)
To determine the nature and characteristics of a unique hemoglobin variant that causes a spurious increase in glycated hemoglobin (HbA1c).Blood specimens from four unrelated persons with this hemoglobin variant were examined by conventional laborator