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Cell
|
June 17, 1988
Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutation
N C Cross, D R Tolan, T M Cox
Nucleic Acids Research
|
April 11, 1990
A new aldolase B variant, N334K, is a common cause of hereditary fructose intolerance in Yugoslavia
N C Cross, L M Stojanov, T M Cox
Leukemia
|
March 10, 2001
Mutations of the transcription factor AML1/CBFA2 are uncommon in blastic transformation of chronic myeloid leukaemia
E J Steer, J M Goldman, N C Cross
Medizinische Klinik (Munich, Germany : 1983)
|
June 22, 1999
[The 8p11 myeloproliferative syndrome]
A Reither, R Hehlmann, J M Goldman, et al.
Cytogenetics and Cell Genetics
|
July 15, 2000
Cloning of ZNF237, a novel member of the MYM gene family that maps to human chromosome 13q11-->q12
J Sohal, A Reiter, J M Goldman, et al.
Leukemia & Lymphoma
|
January 1, 1993
Minimal residual disease after bone marrow transplant for chronic myeloid leukaemia detected by the polymerase chain reaction
N C Cross, L Feng, J Bungey, et al.
Cytogenetics and Cell Genetics
|
August 18, 1999
Assignment of ZNF262 to human chromosome band 1p34-->p32 by in situ hybridization
J Sohal, A Chase, J M Goldman, et al.
Leukemia
|
January 1, 1994
An optimized multiplex polymerase chain reaction (PCR) for detection of BCR-ABL fusion mRNAs in haematological disorders
N C Cross, J V Melo, L Feng, et al.
Blood
|
May 15, 1996
Kinetics of increasing BCR-ABL transcript numbers in chronic myeloid leukemia patients who relapse after bone marrow transplantation
F Lin, F van Rhee, J M Goldman, et al.
Leukemia
|
February 1, 1997
The commonly deleted region at 9p21-22 in lymphoblastic leukemias spans at least 400 kb and includes p16 but not p15 or the IFN gene cluster
R C Aguiar, H Sill, J M Goldman, et al.
Page
of 12
Search research articles
Search
Showing results (21-30 of 115) with videos related to
Sort By:
Page
of 12
Cell
|
June 17, 1988
Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutation
N C Cross, D R Tolan, T M Cox
Nucleic Acids Research
|
April 11, 1990
A new aldolase B variant, N334K, is a common cause of hereditary fructose intolerance in Yugoslavia
N C Cross, L M Stojanov, T M Cox
Leukemia
|
March 10, 2001
Mutations of the transcription factor AML1/CBFA2 are uncommon in blastic transformation of chronic myeloid leukaemia
E J Steer, J M Goldman, N C Cross
Medizinische Klinik (Munich, Germany : 1983)
|
June 22, 1999
[The 8p11 myeloproliferative syndrome]
A Reither, R Hehlmann, J M Goldman, et al.
Cytogenetics and Cell Genetics
|
July 15, 2000
Cloning of ZNF237, a novel member of the MYM gene family that maps to human chromosome 13q11-->q12
J Sohal, A Reiter, J M Goldman, et al.
Leukemia & Lymphoma
|
January 1, 1993
Minimal residual disease after bone marrow transplant for chronic myeloid leukaemia detected by the polymerase chain reaction
N C Cross, L Feng, J Bungey, et al.
Cytogenetics and Cell Genetics
|
August 18, 1999
Assignment of ZNF262 to human chromosome band 1p34-->p32 by in situ hybridization
J Sohal, A Chase, J M Goldman, et al.
Leukemia
|
January 1, 1994
An optimized multiplex polymerase chain reaction (PCR) for detection of BCR-ABL fusion mRNAs in haematological disorders
N C Cross, J V Melo, L Feng, et al.
Blood
|
May 15, 1996
Kinetics of increasing BCR-ABL transcript numbers in chronic myeloid leukemia patients who relapse after bone marrow transplantation
F Lin, F van Rhee, J M Goldman, et al.
Leukemia
|
February 1, 1997
The commonly deleted region at 9p21-22 in lymphoblastic leukemias spans at least 400 kb and includes p16 but not p15 or the IFN gene cluster
R C Aguiar, H Sill, J M Goldman, et al.
Page
of 12