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British Journal of Haematology
|
December 1, 1985
The Ava II psi beta polymorphism is linked to the common Mediterranean beta + thalassaemia mutation
S L Thein, J S Wainscoat, J M Old, et al.
Clinical Genetics
|
May 1, 1986
Detection and exclusion of carriers of ornithine transcarbamylase deficiency by RFLP analysis
M Schwartz, E Christensen, N C Christensen, et al.
Human Heredity
|
July 1, 1995
Spectrum of beta-thalassaemia mutations in the population of Saudi Arabia
F H Hasounah, S A Sejeny, J A Omer, et al.
Nucleic Acids Research
|
December 21, 1981
Restriction mapping of a new deletion responsible for G gamma (delta beta)o thalassemia
R W Jones, J M Old, R J Trent, et al.
Lancet (London, England)
|
December 25, 1982
First-trimester fetal diagnosis for haemoglobinopathies: three cases
J M Old, R H Ward, M Petrou, et al.
British Journal of Haematology
|
March 1, 1982
Restriction endonuclease maps of the beta-like globin gene cluster in the British and Greek forms of HPFH, and for one example of G gamma beta + HPFH
R W Jones, J M Old, W G Wood, et al.
Hemoglobin
|
February 24, 2001
Hb Watford [beta1(NA1)Val-->Gly]: a new, clinically silent hemoglobin variant in linkage with a new neutral mutation
C Fisher, J Hanslip, B N Green, et al.
Cell
|
October 1, 1978
Human globin gene expression: control of beta, delta and delta beta chain production
W G Wood, J M Old, A V Roberts, et al.
Journal of Medical Genetics
|
January 1, 1994
The spectrum of beta thalassaemia mutations in the UAE national population
R Quaife, L al-Gazali, S Abbes, et al.
British Journal of Haematology
|
June 1, 1984
Population and genetic studies suggest a single origin for the Indian deletion beta thalassaemia
S L Thein, J M Old, J S Wainscoat, et al.
Page
of 10
Search research articles
Search
Showing results (61-70 of 99) with videos related to
Sort By:
Page
of 10
British Journal of Haematology
|
December 1, 1985
The Ava II psi beta polymorphism is linked to the common Mediterranean beta + thalassaemia mutation
S L Thein, J S Wainscoat, J M Old, et al.
Clinical Genetics
|
May 1, 1986
Detection and exclusion of carriers of ornithine transcarbamylase deficiency by RFLP analysis
M Schwartz, E Christensen, N C Christensen, et al.
Human Heredity
|
July 1, 1995
Spectrum of beta-thalassaemia mutations in the population of Saudi Arabia
F H Hasounah, S A Sejeny, J A Omer, et al.
Nucleic Acids Research
|
December 21, 1981
Restriction mapping of a new deletion responsible for G gamma (delta beta)o thalassemia
R W Jones, J M Old, R J Trent, et al.
Lancet (London, England)
|
December 25, 1982
First-trimester fetal diagnosis for haemoglobinopathies: three cases
J M Old, R H Ward, M Petrou, et al.
British Journal of Haematology
|
March 1, 1982
Restriction endonuclease maps of the beta-like globin gene cluster in the British and Greek forms of HPFH, and for one example of G gamma beta + HPFH
R W Jones, J M Old, W G Wood, et al.
Hemoglobin
|
February 24, 2001
Hb Watford [beta1(NA1)Val-->Gly]: a new, clinically silent hemoglobin variant in linkage with a new neutral mutation
C Fisher, J Hanslip, B N Green, et al.
Cell
|
October 1, 1978
Human globin gene expression: control of beta, delta and delta beta chain production
W G Wood, J M Old, A V Roberts, et al.
Journal of Medical Genetics
|
January 1, 1994
The spectrum of beta thalassaemia mutations in the UAE national population
R Quaife, L al-Gazali, S Abbes, et al.
British Journal of Haematology
|
June 1, 1984
Population and genetic studies suggest a single origin for the Indian deletion beta thalassaemia
S L Thein, J M Old, J S Wainscoat, et al.
Page
of 10