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Lancet (London, England)
|
October 31, 1992
Factor VIII gene explains all cases of haemophilia A
J A Naylor, P M Green, C R Rizza, et al.
Genetic Testing
|
January 1, 1997
Mutation analysis and genetic service: the construction and use of national confidential databases of mutations and pedigrees
P M Green, N H Waseem, R D Bagnall, et al.
Human Molecular Genetics
|
November 1, 1993
Characteristic mRNA abnormality found in half the patients with severe haemophilia A is due to large DNA inversions
J Naylor, A Brinke, S Hassock, et al.
European Journal of Haematology
|
October 1, 1992
Antenatal diagnosis of haemophilia B by amplification and electrophoresis of an exon fragment with a short deletion
R Ljung, P Green, E Sjörin, et al.
Thrombosis and Haemostasis
|
June 30, 1989
The use of DNA amplification for genetic counselling related diagnosis in haemophilia B
T C Tsang, D R Bentley, I M Nilsson, et al.
Journal of Cell Science
|
February 1, 1978
Changes induced by ultraviolet light in the superhelical DNA of lymphocytes from subjects with xeroderma pigmentosum and normal controls
P R Cook, I A Brazell, S A Pawsey, et al.
Nature: New Biology
|
September 20, 1972
Induction of galactokinase in fibroblasts from heterozygous and homozygous subjects
F Zacchello, P F Benson, S Brown, et al.
Bollettino Dell'Istituto Sieroterapico Milanese
|
November 30, 1980
[Epidemiological considerations on 289 cases of tetanus]
L Caggese, M R Villa, I Schlacht, et al.
The EMBO Journal
|
October 1, 1988
A factor IX mutation, verified by direct genomic sequencing, causes haemophilia B by a novel mechanism
T C Tsang, D R Bentley, R S Mibashan, et al.
Journal of the American Academy of Dermatology
|
May 1, 1988
Xeroderma pigmentosum complementation group F in a non-Japanese patient
P G Norris, J L Hawk, J A Avery, et al.
Page
of 14
Search research articles
Search
Showing results (61-70 of 140) with videos related to
Sort By:
Page
of 14
Lancet (London, England)
|
October 31, 1992
Factor VIII gene explains all cases of haemophilia A
J A Naylor, P M Green, C R Rizza, et al.
Genetic Testing
|
January 1, 1997
Mutation analysis and genetic service: the construction and use of national confidential databases of mutations and pedigrees
P M Green, N H Waseem, R D Bagnall, et al.
Human Molecular Genetics
|
November 1, 1993
Characteristic mRNA abnormality found in half the patients with severe haemophilia A is due to large DNA inversions
J Naylor, A Brinke, S Hassock, et al.
European Journal of Haematology
|
October 1, 1992
Antenatal diagnosis of haemophilia B by amplification and electrophoresis of an exon fragment with a short deletion
R Ljung, P Green, E Sjörin, et al.
Thrombosis and Haemostasis
|
June 30, 1989
The use of DNA amplification for genetic counselling related diagnosis in haemophilia B
T C Tsang, D R Bentley, I M Nilsson, et al.
Journal of Cell Science
|
February 1, 1978
Changes induced by ultraviolet light in the superhelical DNA of lymphocytes from subjects with xeroderma pigmentosum and normal controls
P R Cook, I A Brazell, S A Pawsey, et al.
Nature: New Biology
|
September 20, 1972
Induction of galactokinase in fibroblasts from heterozygous and homozygous subjects
F Zacchello, P F Benson, S Brown, et al.
Bollettino Dell'Istituto Sieroterapico Milanese
|
November 30, 1980
[Epidemiological considerations on 289 cases of tetanus]
L Caggese, M R Villa, I Schlacht, et al.
The EMBO Journal
|
October 1, 1988
A factor IX mutation, verified by direct genomic sequencing, causes haemophilia B by a novel mechanism
T C Tsang, D R Bentley, R S Mibashan, et al.
Journal of the American Academy of Dermatology
|
May 1, 1988
Xeroderma pigmentosum complementation group F in a non-Japanese patient
P G Norris, J L Hawk, J A Avery, et al.
Page
of 14