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Journal of Pediatric Hematology/Oncology
|
February 1, 1996
Recurrent human parvovirus B19-induced anemia: initial manifestation of humoral immunodeficiency
J C Murray, M E Paul, H M Rosenblatt, et al.
Nucleic Acids Research
|
January 12, 1987
An anonymous genomic clone that detects a frequent RFLP adjacent to the D4S10 (G8) marker and Huntington's disease
L R Carlock, T D Vo, C R DeHaven, et al.
Nucleic Acids Research
|
April 11, 1991
An EcoO109 RFLP for the SNRPE gene on chromosome 1
B L Miller, D Y Nishimura, E D Wieben, et al.
Journal of Chromatography
|
April 6, 1990
Determination of collagen and protein turnover by high-performance liquid chromatography
M R Stratford, R R Watfa, J C Murray, et al.
Genomics
|
September 1, 1990
A detailed multipoint gene map of chromosome 1q
K H Buetow, D Nishimura, Y Nakamura, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
July 31, 1998
Infant TGF-alpha genotype, orofacial clefts, and maternal periconceptional multivitamin use
G M Shaw, C R Wasserman, J C Murray, et al.
Proceedings of the Finnish Dental Society. Suomen Hammaslaakariseuran Toimituksia
|
January 1, 1992
Genetic marker study of dentinogenesis imperfecta
M G Crall, C F Schuler, K H Buetow, et al.
The Pediatric Infectious Disease Journal
|
November 1, 1996
Chronic osteomyelitis caused by Clostridium difficile in an adolescent with sickle cell disease
M J Gaglani, J C Murray, A B Morad, et al.
Hemoglobin
|
January 1, 1983
Restriction endonuclease mapping of globin genomic regions of HEL (human erythroleukemia) line
R F Mueller, J C Murray, R Gelinas, et al.
Bone Marrow Transplantation
|
June 1, 1995
Epiglottitis following preparation for allogeneic bone marrow transplantation
J C Murray, J K Chiu, S R Dorfman, et al.
Page
of 33
Search research articles
Search
Showing results (151-160 of 328) with videos related to
Sort By:
Page
of 33
Journal of Pediatric Hematology/Oncology
|
February 1, 1996
Recurrent human parvovirus B19-induced anemia: initial manifestation of humoral immunodeficiency
J C Murray, M E Paul, H M Rosenblatt, et al.
Nucleic Acids Research
|
January 12, 1987
An anonymous genomic clone that detects a frequent RFLP adjacent to the D4S10 (G8) marker and Huntington's disease
L R Carlock, T D Vo, C R DeHaven, et al.
Nucleic Acids Research
|
April 11, 1991
An EcoO109 RFLP for the SNRPE gene on chromosome 1
B L Miller, D Y Nishimura, E D Wieben, et al.
Journal of Chromatography
|
April 6, 1990
Determination of collagen and protein turnover by high-performance liquid chromatography
M R Stratford, R R Watfa, J C Murray, et al.
Genomics
|
September 1, 1990
A detailed multipoint gene map of chromosome 1q
K H Buetow, D Nishimura, Y Nakamura, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
July 31, 1998
Infant TGF-alpha genotype, orofacial clefts, and maternal periconceptional multivitamin use
G M Shaw, C R Wasserman, J C Murray, et al.
Proceedings of the Finnish Dental Society. Suomen Hammaslaakariseuran Toimituksia
|
January 1, 1992
Genetic marker study of dentinogenesis imperfecta
M G Crall, C F Schuler, K H Buetow, et al.
The Pediatric Infectious Disease Journal
|
November 1, 1996
Chronic osteomyelitis caused by Clostridium difficile in an adolescent with sickle cell disease
M J Gaglani, J C Murray, A B Morad, et al.
Hemoglobin
|
January 1, 1983
Restriction endonuclease mapping of globin genomic regions of HEL (human erythroleukemia) line
R F Mueller, J C Murray, R Gelinas, et al.
Bone Marrow Transplantation
|
June 1, 1995
Epiglottitis following preparation for allogeneic bone marrow transplantation
J C Murray, J K Chiu, S R Dorfman, et al.
Page
of 33