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Annals of the New York Academy of Sciences
|
January 1, 1980
Molecular mechanisms in alpha thalassemia: racial differences in alpha-globin gene organization
S H Embury, A M Dozy, Y W Kan
Birth Defects Original Article Series
|
January 1, 1982
Prenatal diagnosis by DNA analysis
Y W Kan, J C Chang, A M Dozy
The New England Journal of Medicine
|
November 17, 1977
Identification of a nondeletion defect in alpha-thalassemia
Y W Kan, A M Dozy, R Trecartin, et al.
The New England Journal of Medicine
|
May 22, 1975
Successful application of prenatal diagnosis in a pregnancy at risk for homozygous beta-thalassemia
Y W Kan, M S Golbus, P Klein, et al.
Annals of the New York Academy of Sciences
|
January 1, 1990
The use of direct gene analysis to define beta-thalassemia
A M Dozy, S P Cai, F Chehab, et al.
Lancet (London, England)
|
January 7, 1984
A rapid screening test for antenatal sex determination
Y F Lau, J C Huang, A M Dozy, et al.
Human Mutation
|
January 1, 1994
A new frameshift mutation, insertion of ATCT, at codon 48 in the beta-globin gene causes beta-thalassemia in an Indian proband
P K Jain, A M Dozy, I C Verma, et al.
Nature
|
April 8, 1982
Construction of a functional human suppressor tRNA gene: an approach to gene therapy for beta-thalassaemia
G F Temple, A M Dozy, K L Roy, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 1, 1975
Demonstration of non-functional beta-globin mRNA in homozygous beta (0) thalassemia
Y W Kan, J P Holland, A M Dozy, et al.
The Journal of Clinical Investigation
|
June 1, 1979
Organization of the alpha-globin genes in the Chinese alpha-thalassemia syndromes
S H Embury, R V Lebo, A M Dozy, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 41) with videos related to
Sort By:
Page
of 5
Annals of the New York Academy of Sciences
|
January 1, 1980
Molecular mechanisms in alpha thalassemia: racial differences in alpha-globin gene organization
S H Embury, A M Dozy, Y W Kan
Birth Defects Original Article Series
|
January 1, 1982
Prenatal diagnosis by DNA analysis
Y W Kan, J C Chang, A M Dozy
The New England Journal of Medicine
|
November 17, 1977
Identification of a nondeletion defect in alpha-thalassemia
Y W Kan, A M Dozy, R Trecartin, et al.
The New England Journal of Medicine
|
May 22, 1975
Successful application of prenatal diagnosis in a pregnancy at risk for homozygous beta-thalassemia
Y W Kan, M S Golbus, P Klein, et al.
Annals of the New York Academy of Sciences
|
January 1, 1990
The use of direct gene analysis to define beta-thalassemia
A M Dozy, S P Cai, F Chehab, et al.
Lancet (London, England)
|
January 7, 1984
A rapid screening test for antenatal sex determination
Y F Lau, J C Huang, A M Dozy, et al.
Human Mutation
|
January 1, 1994
A new frameshift mutation, insertion of ATCT, at codon 48 in the beta-globin gene causes beta-thalassemia in an Indian proband
P K Jain, A M Dozy, I C Verma, et al.
Nature
|
April 8, 1982
Construction of a functional human suppressor tRNA gene: an approach to gene therapy for beta-thalassaemia
G F Temple, A M Dozy, K L Roy, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 1, 1975
Demonstration of non-functional beta-globin mRNA in homozygous beta (0) thalassemia
Y W Kan, J P Holland, A M Dozy, et al.
The Journal of Clinical Investigation
|
June 1, 1979
Organization of the alpha-globin genes in the Chinese alpha-thalassemia syndromes
S H Embury, R V Lebo, A M Dozy, et al.
Page
of 5