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The Journal of Gene Medicine
|
February 7, 2001
Closed hollow-fiber bioreactor: a new approach to retroviral vector production
D Pan, C B Whitley
The New England Journal of Medicine
|
April 23, 1987
Bone marrow transplantation for genetic diseases
W Krivit, C B Whitley
Human Genetics
|
November 1, 1992
Assessment of iduronate-2-sulfatase mRNA expression in Hunter syndrome (mucopolysaccharidosis type II)
P L Crotty, C B Whitley
American Journal of Medical Genetics
|
September 1, 1991
Adams-Oliver syndrome revisited
C B Whitley, R J Gorlin
Radiology
|
September 1, 1983
Achondrogenesis: new nosology with evidence of genetic heterogeneity
C B Whitley, R J Gorlin
Radiology
|
October 1, 1983
Lenz-Majewski syndrome
R J Gorlin, C B Whitley
Human Gene Therapy
|
October 30, 1999
Real-time quantitative polymerase chain reaction to assess gene transfer
K Becker, D Pan, C B Whitley
American Journal of Medical Genetics
|
September 1, 1987
A nonpathologic allele (IW) for low alpha-L-iduronidase enzyme activity vis-a-vis prenatal diagnosis of Hurler syndrome
C B Whitley, R J Gorlin, W Krivit
American Journal of Human Genetics
|
January 1, 1996
Molecular genetic defect underlying alpha-L-iduronidase pseudodeficiency
E L Aronovich, D Pan, C B Whitley
Clinical Genetics
|
February 4, 2018
SAAMP 2.0: An algorithm to predict genotype-phenotype correlation of lysosomal storage diseases
L Ou, M J Przybilla, C B Whitley
Page
of 6
Search research articles
Search
Showing results (1-10 of 58) with videos related to
Sort By:
Page
of 6
The Journal of Gene Medicine
|
February 7, 2001
Closed hollow-fiber bioreactor: a new approach to retroviral vector production
D Pan, C B Whitley
The New England Journal of Medicine
|
April 23, 1987
Bone marrow transplantation for genetic diseases
W Krivit, C B Whitley
Human Genetics
|
November 1, 1992
Assessment of iduronate-2-sulfatase mRNA expression in Hunter syndrome (mucopolysaccharidosis type II)
P L Crotty, C B Whitley
American Journal of Medical Genetics
|
September 1, 1991
Adams-Oliver syndrome revisited
C B Whitley, R J Gorlin
Radiology
|
September 1, 1983
Achondrogenesis: new nosology with evidence of genetic heterogeneity
C B Whitley, R J Gorlin
Radiology
|
October 1, 1983
Lenz-Majewski syndrome
R J Gorlin, C B Whitley
Human Gene Therapy
|
October 30, 1999
Real-time quantitative polymerase chain reaction to assess gene transfer
K Becker, D Pan, C B Whitley
American Journal of Medical Genetics
|
September 1, 1987
A nonpathologic allele (IW) for low alpha-L-iduronidase enzyme activity vis-a-vis prenatal diagnosis of Hurler syndrome
C B Whitley, R J Gorlin, W Krivit
American Journal of Human Genetics
|
January 1, 1996
Molecular genetic defect underlying alpha-L-iduronidase pseudodeficiency
E L Aronovich, D Pan, C B Whitley
Clinical Genetics
|
February 4, 2018
SAAMP 2.0: An algorithm to predict genotype-phenotype correlation of lysosomal storage diseases
L Ou, M J Przybilla, C B Whitley
Page
of 6