Search research articles
Contact Us
Filters
Showing results (21-30 of 38) with videos related to
Page
of 4
Sort By:
Pediatric Infectious Disease
|
January 1, 1985
An unusual case of intracranial suppuration
C G Prober, L K Bachrach, R P Humphreys, et al.
Arthritis and Rheumatism
|
May 1, 1983
Calcium pyrophosphate dihydrate crystal deposition disease with concurrent vertebral hyperostosis in a Barbary ape
R A Kandel, R C Renlund, P T Cheng, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
October 16, 2004
Frequency and heritability of WT1 mutations in nonsyndromic Wilms' tumor patients: a UK Children's Cancer Study Group Study
Suzanne E Little, Sandra P Hanks, Linda King-Underwood, et al.
The Lancet. Oncology
|
June 3, 2004
Genetic predisposition to testicular germ-cell tumours
M F Lutke Holzik, E A Rapley, H J Hoekstra, et al.
American Journal of Medical Genetics
|
December 26, 2001
Case of interstitial 12q deletion in association with Wilms tumor
E A Rapley, D Hargrave, N Persinguhe, et al.
Genes, Chromosomes & Cancer
|
October 19, 2007
Somatic KIT mutations occur predominantly in seminoma germ cell tumors and are not predictive of bilateral disease: report of 220 tumors and review of literature
Jerome Coffey, Rachel Linger, Julia Pugh, et al.
Stem Cells (Dayton, Ohio)
|
January 11, 2016
A Primitive Growth Factor, NME7AB , Is Sufficient to Induce Stable Naïve State Human Pluripotency; Reprogramming in This Novel Growth Factor Confers Superior Differentiation
M G Carter, B J Smagghe, A K Stewart, et al.
British Journal of Cancer
|
November 1, 2007
Testicular microlithiasis as a familial risk factor for testicular germ cell tumour
J Coffey, R A Huddart, F Elliott, et al.
Nature Genetics
|
June 15, 2010
Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer
Clare Turnbull, Elizabeth A Rapley, Sheila Seal, et al.
British Journal of Cancer
|
July 20, 2000
Evidence for susceptibility genes to familial Wilms tumour in addition to WT1, FWT1 and FWT2
E A Rapley, R Barfoot, C Bonaïti-Pellié, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 38) with videos related to
Sort By:
Page
of 4
Pediatric Infectious Disease
|
January 1, 1985
An unusual case of intracranial suppuration
C G Prober, L K Bachrach, R P Humphreys, et al.
Arthritis and Rheumatism
|
May 1, 1983
Calcium pyrophosphate dihydrate crystal deposition disease with concurrent vertebral hyperostosis in a Barbary ape
R A Kandel, R C Renlund, P T Cheng, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
October 16, 2004
Frequency and heritability of WT1 mutations in nonsyndromic Wilms' tumor patients: a UK Children's Cancer Study Group Study
Suzanne E Little, Sandra P Hanks, Linda King-Underwood, et al.
The Lancet. Oncology
|
June 3, 2004
Genetic predisposition to testicular germ-cell tumours
M F Lutke Holzik, E A Rapley, H J Hoekstra, et al.
American Journal of Medical Genetics
|
December 26, 2001
Case of interstitial 12q deletion in association with Wilms tumor
E A Rapley, D Hargrave, N Persinguhe, et al.
Genes, Chromosomes & Cancer
|
October 19, 2007
Somatic KIT mutations occur predominantly in seminoma germ cell tumors and are not predictive of bilateral disease: report of 220 tumors and review of literature
Jerome Coffey, Rachel Linger, Julia Pugh, et al.
Stem Cells (Dayton, Ohio)
|
January 11, 2016
A Primitive Growth Factor, NME7AB , Is Sufficient to Induce Stable Naïve State Human Pluripotency; Reprogramming in This Novel Growth Factor Confers Superior Differentiation
M G Carter, B J Smagghe, A K Stewart, et al.
British Journal of Cancer
|
November 1, 2007
Testicular microlithiasis as a familial risk factor for testicular germ cell tumour
J Coffey, R A Huddart, F Elliott, et al.
Nature Genetics
|
June 15, 2010
Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer
Clare Turnbull, Elizabeth A Rapley, Sheila Seal, et al.
British Journal of Cancer
|
July 20, 2000
Evidence for susceptibility genes to familial Wilms tumour in addition to WT1, FWT1 and FWT2
E A Rapley, R Barfoot, C Bonaïti-Pellié, et al.
Page
of 4