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Medical Image Analysis
|
March 6, 2007
An atlas-based method to compensate for brain shift: preliminary results
Prashanth Dumpuri, Reid C Thompson, Benoit M Dawant, et al.
Journal of Perinatal Medicine
|
January 1, 1991
Early antenatal sonographic diagnosis of conjoined syncephalus-craniothoraco-omphalopagus twins. Case report
G Monni, C Useli, R M Ibba, et al.
Journal of Medical Genetics
|
June 1, 1987
Beta thalassaemia mutations in the Turkish population
N Akar, A O Cavdar, E Dessi, et al.
British Journal of Haematology
|
April 1, 1980
Interaction between the glucose-6-phosphate dehydrogenase deficiency and thalassaemia genes at phenotype level
G Sanna, F Frau, M A Melis, et al.
Blood Cells, Molecules & Diseases
|
November 27, 1999
Activation of the delta-globin gene by the beta-globin gene CACCC motif
M S Ristaldi, S Casula, S Porcu, et al.
British Journal of Haematology
|
December 1, 1983
Phenotypic manifestations of heterozygous non-deletion alpha-thalassaemia (alpha alpha/(alpha alpha)th) in Sardinians
R Galanello, E Paglietti, L Giagu, et al.
The Indian Journal of Medical Research
|
May 4, 2000
A beta-thalassaemia allele with 3 base substitution in codons 4/5 & 6 (ACT CCT GAG-> ACA TCT TAG) detected by denaturing gradient gel electrophoresis & sequencing
R Saxena, L Moi, M Demurtas, et al.
The Journal of Biological Chemistry
|
June 27, 1997
hMAF, a small human transcription factor that heterodimerizes specifically with Nrf1 and Nrf2
M G Marini, K Chan, L Casula, et al.
International Ophthalmology
|
November 10, 2024
Clinical Outcomes of Infectious Keratitis Associated with Contact Lens Wear Following Penetrating Keratoplasty: A Case Series
Angela A Cao, Dylan Stevens, Victoria Miller, et al.
Cancer Genetics and Cytogenetics
|
August 1, 1987
Acute lymphoblastic leukemia in a child with constitutional ring chromosome 21
A M Falchi, M G Orofino, A L Nucaro, et al.
Page
of 47
Search research articles
Search
Showing results (201-210 of 461) with videos related to
Sort By:
Page
of 47
Medical Image Analysis
|
March 6, 2007
An atlas-based method to compensate for brain shift: preliminary results
Prashanth Dumpuri, Reid C Thompson, Benoit M Dawant, et al.
Journal of Perinatal Medicine
|
January 1, 1991
Early antenatal sonographic diagnosis of conjoined syncephalus-craniothoraco-omphalopagus twins. Case report
G Monni, C Useli, R M Ibba, et al.
Journal of Medical Genetics
|
June 1, 1987
Beta thalassaemia mutations in the Turkish population
N Akar, A O Cavdar, E Dessi, et al.
British Journal of Haematology
|
April 1, 1980
Interaction between the glucose-6-phosphate dehydrogenase deficiency and thalassaemia genes at phenotype level
G Sanna, F Frau, M A Melis, et al.
Blood Cells, Molecules & Diseases
|
November 27, 1999
Activation of the delta-globin gene by the beta-globin gene CACCC motif
M S Ristaldi, S Casula, S Porcu, et al.
British Journal of Haematology
|
December 1, 1983
Phenotypic manifestations of heterozygous non-deletion alpha-thalassaemia (alpha alpha/(alpha alpha)th) in Sardinians
R Galanello, E Paglietti, L Giagu, et al.
The Indian Journal of Medical Research
|
May 4, 2000
A beta-thalassaemia allele with 3 base substitution in codons 4/5 & 6 (ACT CCT GAG-> ACA TCT TAG) detected by denaturing gradient gel electrophoresis & sequencing
R Saxena, L Moi, M Demurtas, et al.
The Journal of Biological Chemistry
|
June 27, 1997
hMAF, a small human transcription factor that heterodimerizes specifically with Nrf1 and Nrf2
M G Marini, K Chan, L Casula, et al.
International Ophthalmology
|
November 10, 2024
Clinical Outcomes of Infectious Keratitis Associated with Contact Lens Wear Following Penetrating Keratoplasty: A Case Series
Angela A Cao, Dylan Stevens, Victoria Miller, et al.
Cancer Genetics and Cytogenetics
|
August 1, 1987
Acute lymphoblastic leukemia in a child with constitutional ring chromosome 21
A M Falchi, M G Orofino, A L Nucaro, et al.
Page
of 47