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Human Mutation
|
January 1, 1995
Rapid DNA haplotyping using a multiplex heteroduplex approach: application to Duchenne muscular dystrophy carrier testing
T W Prior, G D Wenger, A C Papp, et al.
Clinical Chemistry
|
January 1, 1995
A molecular protocol for diagnosing myotonic dystrophy
M Guida, R S Marger, A C Papp, et al.
Transplantation
|
June 27, 1994
Detection of cytomegalovirus in liver transplant biopsies. A comparison of light microscopy, immunohistochemistry, duplex PCR and nested PCR
J A Brainard, J K Greenson, C J Vesy, et al.
Clinical Chemistry
|
December 1, 1990
Determination of carrier status in Duchenne and Becker muscular dystrophies by quantitative polymerase chain reaction and allele-specific oligonucleotides
T W Prior, A C Papp, P J Snyder, et al.
Neurology
|
February 1, 1997
Dystrophin expression in a Duchenne muscular dystrophy patient with a frame shift deletion
T W Prior, C Bartolo, A C Papp, et al.
Gastroenterology
|
December 31, 1998
The I1307K polymorphism of the APC gene in colorectal cancer
T W Prior, R B Chadwick, A C Papp, et al.
Human Genetics
|
April 3, 2001
Hybrids monosomal for human chromosome 5 reveal the presence of a spinal muscular atrophy (SMA) carrier with two SMN1 copies on one chromosome
M D Mailman, T Hemingway, R L Darsey, et al.
Clinical Pharmacology and Therapeutics
|
October 2, 2013
Cholesteryl ester transfer protein polymorphisms, statin use, and their impact on cholesterol levels and cardiovascular events
M Leusink, N C Onland-Moret, F W Asselbergs, et al.
The Pharmacogenomics Journal
|
February 10, 2016
Transcriptomic variation of pharmacogenes in multiple human tissues and lymphoblastoid cell lines
A Chhibber, C E French, S W Yee, et al.
Page
of 4
Search research articles
Search
Showing results (31-40 of 39) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 39 results.
Human Mutation
|
January 1, 1995
Rapid DNA haplotyping using a multiplex heteroduplex approach: application to Duchenne muscular dystrophy carrier testing
T W Prior, G D Wenger, A C Papp, et al.
Clinical Chemistry
|
January 1, 1995
A molecular protocol for diagnosing myotonic dystrophy
M Guida, R S Marger, A C Papp, et al.
Transplantation
|
June 27, 1994
Detection of cytomegalovirus in liver transplant biopsies. A comparison of light microscopy, immunohistochemistry, duplex PCR and nested PCR
J A Brainard, J K Greenson, C J Vesy, et al.
Clinical Chemistry
|
December 1, 1990
Determination of carrier status in Duchenne and Becker muscular dystrophies by quantitative polymerase chain reaction and allele-specific oligonucleotides
T W Prior, A C Papp, P J Snyder, et al.
Neurology
|
February 1, 1997
Dystrophin expression in a Duchenne muscular dystrophy patient with a frame shift deletion
T W Prior, C Bartolo, A C Papp, et al.
Gastroenterology
|
December 31, 1998
The I1307K polymorphism of the APC gene in colorectal cancer
T W Prior, R B Chadwick, A C Papp, et al.
Human Genetics
|
April 3, 2001
Hybrids monosomal for human chromosome 5 reveal the presence of a spinal muscular atrophy (SMA) carrier with two SMN1 copies on one chromosome
M D Mailman, T Hemingway, R L Darsey, et al.
Clinical Pharmacology and Therapeutics
|
October 2, 2013
Cholesteryl ester transfer protein polymorphisms, statin use, and their impact on cholesterol levels and cardiovascular events
M Leusink, N C Onland-Moret, F W Asselbergs, et al.
The Pharmacogenomics Journal
|
February 10, 2016
Transcriptomic variation of pharmacogenes in multiple human tissues and lymphoblastoid cell lines
A Chhibber, C E French, S W Yee, et al.
Page
of 4