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Biochimica Et Biophysica Acta
|
June 5, 1986
Hb J-Antakya or alpha 2 beta (2)65(E9)Lys----Met in a Turkish family and Hb complutense or alpha 2 beta (2)127(H5)Gln----Glu in a Spanish family; correction of a previously published identification
T H Huisman, J B Wilson, A Kutlar, et al.
Transplantation Proceedings
|
April 15, 2019
The Analysis of Posthepatectomy Liver Failure Incidence and Risk Factors Among Right Liver Living Donors According to International Study Group of Liver Surgery Definition
T Egeli, T Unek, C Agalar, et al.
Hemoglobin
|
January 1, 1989
A search for anomalies in the zeta, alpha, beta, and gamma globin gene arrangements in normal black, Italian, Turkish, and Spanish newborns
Y J Fei, F Kutlar, H F Harris, et al.
Hemoglobin
|
January 1, 1990
Beta-thalassemia in Turkey
R Oner, C Altay, A Gurgey, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
January 13, 2016
Familial partial lipodystrophy linked to a novel peroxisome proliferator activator receptor -γ (PPARG) mutation, H449L: a comparison of people with this mutation and those with classic codon 482 Lamin A/C (LMNA) mutations
T Demir, H Onay, D B Savage, et al.
Biochimica Et Biophysica Acta
|
August 23, 1996
The relative levels of alpha 2-, alpha 1-, and zeta-mRNA in HB H patients with different deletional and nondeletional alpha-thalassemia determinants
N S Smetanina, C Oner, E Baysal, et al.
Biochemical and Biophysical Research Communications
|
June 16, 1988
Beta-thalassemia due to a T----A mutation within the ATA box
Y J Fei, T A Stoming, G D Efremov, et al.
Blood
|
January 1, 1988
Mild and severe beta-thalassemia among homozygotes from Turkey: identification of the types by hybridization of amplified DNA with synthetic probes
J C Diaz-Chico, K G Yang, T A Stoming, et al.
British Journal of Haematology
|
April 1, 1994
Possible factors influencing the haemoglobin and fetal haemoglobin levels in patients with beta-thalassaemia due to a homozygosity for the IVS-I-6 (T-->C) mutation
D G Efremov, A J Dimovski, E Baysal, et al.
Human Genetics
|
April 1, 1992
Beta S haplotypes in various world populations
C Oner, A J Dimovski, N F Olivieri, et al.
Page
of 16
Search research articles
Search
Showing results (141-150 of 160) with videos related to
Sort By:
Page
of 16
Biochimica Et Biophysica Acta
|
June 5, 1986
Hb J-Antakya or alpha 2 beta (2)65(E9)Lys----Met in a Turkish family and Hb complutense or alpha 2 beta (2)127(H5)Gln----Glu in a Spanish family; correction of a previously published identification
T H Huisman, J B Wilson, A Kutlar, et al.
Transplantation Proceedings
|
April 15, 2019
The Analysis of Posthepatectomy Liver Failure Incidence and Risk Factors Among Right Liver Living Donors According to International Study Group of Liver Surgery Definition
T Egeli, T Unek, C Agalar, et al.
Hemoglobin
|
January 1, 1989
A search for anomalies in the zeta, alpha, beta, and gamma globin gene arrangements in normal black, Italian, Turkish, and Spanish newborns
Y J Fei, F Kutlar, H F Harris, et al.
Hemoglobin
|
January 1, 1990
Beta-thalassemia in Turkey
R Oner, C Altay, A Gurgey, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
January 13, 2016
Familial partial lipodystrophy linked to a novel peroxisome proliferator activator receptor -γ (PPARG) mutation, H449L: a comparison of people with this mutation and those with classic codon 482 Lamin A/C (LMNA) mutations
T Demir, H Onay, D B Savage, et al.
Biochimica Et Biophysica Acta
|
August 23, 1996
The relative levels of alpha 2-, alpha 1-, and zeta-mRNA in HB H patients with different deletional and nondeletional alpha-thalassemia determinants
N S Smetanina, C Oner, E Baysal, et al.
Biochemical and Biophysical Research Communications
|
June 16, 1988
Beta-thalassemia due to a T----A mutation within the ATA box
Y J Fei, T A Stoming, G D Efremov, et al.
Blood
|
January 1, 1988
Mild and severe beta-thalassemia among homozygotes from Turkey: identification of the types by hybridization of amplified DNA with synthetic probes
J C Diaz-Chico, K G Yang, T A Stoming, et al.
British Journal of Haematology
|
April 1, 1994
Possible factors influencing the haemoglobin and fetal haemoglobin levels in patients with beta-thalassaemia due to a homozygosity for the IVS-I-6 (T-->C) mutation
D G Efremov, A J Dimovski, E Baysal, et al.
Human Genetics
|
April 1, 1992
Beta S haplotypes in various world populations
C Oner, A J Dimovski, N F Olivieri, et al.
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of 16