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T W Prior

Showing results (61-70 of 75) with videos related to

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Clinical Chemistry|December 1, 1990
Determination of carrier status in Duchenne and Becker muscular dystrophies by quantitative polymerase chain reaction and allele-specific oligonucleotidesT W Prior, A C Papp, P J Snyder, et al.
Human Genetics|August 1, 1996
Mutational spectrum in the neurofibromatosis type 2 gene in sporadic and familial schwannomasD B Welling, M Guida, F Goll, et al.
The New England Journal of Medicine|September 28, 1995
Myoblast transfer in the treatment of Duchenne's muscular dystrophyJ R Mendell, J T Kissel, A A Amato, et al.
Neuropathology and Applied Neurobiology|July 27, 2006
Diagnostic and prognostic value of glycosyltransferase mRNA in glioblastoma multiforme patientsJ L Oblinger, D K Pearl, C L Boardman, et al.
Human Molecular Genetics|August 1, 1997
The survival motor neuron protein in spinal muscular atrophyD D Coovert, T T Le, P E McAndrew, et al.
Neurology|February 1, 1997
Dystrophin expression in a Duchenne muscular dystrophy patient with a frame shift deletionT W Prior, C Bartolo, A C Papp, et al.
Journal of Medical Genetics|July 28, 2001
Hereditary and somatic DNA mismatch repair gene mutations in sporadic endometrial carcinomaR B Chadwick, R E Pyatt, T H Niemann, et al.
Journal of Medical Genetics|June 14, 2000
Over-representation of PPARgamma sequence variants in sporadic cases of glioblastoma multiforme: preliminary evidence for common low penetrance modifiers for brain tumour risk in the general populationX P Zhou, W M Smith, O Gimm, et al.
Human Genetics|August 21, 2001
Opposite association of two PPARG variants with cancer: overrepresentation of H449H in endometrial carcinoma cases and underrepresentation of P12A in renal cell carcinoma casesW M Smith, X P Zhou, K Kurose, et al.
Gastroenterology|December 31, 1998
The I1307K polymorphism of the APC gene in colorectal cancerT W Prior, R B Chadwick, A C Papp, et al.
Pageof 8

Showing results (61-70 of 75) with videos related to

Sort By:
Pageof 8
Clinical Chemistry|December 1, 1990
Determination of carrier status in Duchenne and Becker muscular dystrophies by quantitative polymerase chain reaction and allele-specific oligonucleotidesT W Prior, A C Papp, P J Snyder, et al.
Human Genetics|August 1, 1996
Mutational spectrum in the neurofibromatosis type 2 gene in sporadic and familial schwannomasD B Welling, M Guida, F Goll, et al.
The New England Journal of Medicine|September 28, 1995
Myoblast transfer in the treatment of Duchenne's muscular dystrophyJ R Mendell, J T Kissel, A A Amato, et al.
Neuropathology and Applied Neurobiology|July 27, 2006
Diagnostic and prognostic value of glycosyltransferase mRNA in glioblastoma multiforme patientsJ L Oblinger, D K Pearl, C L Boardman, et al.
Human Molecular Genetics|August 1, 1997
The survival motor neuron protein in spinal muscular atrophyD D Coovert, T T Le, P E McAndrew, et al.
Neurology|February 1, 1997
Dystrophin expression in a Duchenne muscular dystrophy patient with a frame shift deletionT W Prior, C Bartolo, A C Papp, et al.
Journal of Medical Genetics|July 28, 2001
Hereditary and somatic DNA mismatch repair gene mutations in sporadic endometrial carcinomaR B Chadwick, R E Pyatt, T H Niemann, et al.
Journal of Medical Genetics|June 14, 2000
Over-representation of PPARgamma sequence variants in sporadic cases of glioblastoma multiforme: preliminary evidence for common low penetrance modifiers for brain tumour risk in the general populationX P Zhou, W M Smith, O Gimm, et al.
Human Genetics|August 21, 2001
Opposite association of two PPARG variants with cancer: overrepresentation of H449H in endometrial carcinoma cases and underrepresentation of P12A in renal cell carcinoma casesW M Smith, X P Zhou, K Kurose, et al.
Gastroenterology|December 31, 1998
The I1307K polymorphism of the APC gene in colorectal cancerT W Prior, R B Chadwick, A C Papp, et al.
Pageof 8