Search research articles
Contact Us
Filters
Showing results (141-150 of 163) with videos related to
Page
of 17
Sort By:
Journal of the American Society of Nephrology : JASN
|
November 30, 1999
Aberrant splicing in the PKD2 gene as a cause of polycystic kidney disease
D M Reynolds, T Hayashi, Y Cai, et al.
Cytogenetic and Genome Research
|
September 29, 2007
Variation of CNV distribution in five different ethnic populations
S J White, L E L M Vissers, A Geurts van Kessel, et al.
Leukemia
|
February 3, 1998
Detection of CBP rearrangements in acute myelogenous leukemia with t(8;16)
R H Giles, J G Dauwerse, C Higgins, et al.
American Journal of Human Genetics
|
October 27, 1997
A spectrum of mutations in the second gene for autosomal dominant polycystic kidney disease (PKD2)
B Veldhuisen, J J Saris, S de Haij, et al.
Clinical Genetics
|
May 22, 2010
X-chromosome duplications in males with mental retardation: pathogenic or benign variants?
A C J Gijsbers, N S den Hollander, A T J M Helderman-van de Enden, et al.
Neurobiology of Disease
|
October 21, 1999
Targeted disruption of the Cln3 gene provides a mouse model for Batten disease. The Batten Mouse Model Consortium [corrected]
H M Mitchison, D J Bernard, N D Greene, et al.
Kidney International
|
April 12, 2000
Location of mutations within the PKD2 gene influences clinical outcome
N Hateboer, B Veldhuisen, D Peters, et al.
Leukemia
|
September 1, 1996
Simple method for detection of MYH11 DNA rearrangements in patients with inv(16)(p13q22) and acute myeloid leukemia
B A van der Reijden, D Martinet, J G Dauwerse, et al.
Familial Cancer
|
October 24, 2003
Bannayan-Riley-Ruvalcaba syndrome: further delineation of the phenotype and management of PTEN mutation-positive cases
Y M C Hendriks, J T C M Verhallen, J J van der Smagt, et al.
Journal of Medical Genetics
|
June 14, 2008
Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant
F D Hannes, A J Sharp, H C Mefford, et al.
Page
of 17
Search research articles
Search
Showing results (141-150 of 163) with videos related to
Sort By:
Page
of 17
Journal of the American Society of Nephrology : JASN
|
November 30, 1999
Aberrant splicing in the PKD2 gene as a cause of polycystic kidney disease
D M Reynolds, T Hayashi, Y Cai, et al.
Cytogenetic and Genome Research
|
September 29, 2007
Variation of CNV distribution in five different ethnic populations
S J White, L E L M Vissers, A Geurts van Kessel, et al.
Leukemia
|
February 3, 1998
Detection of CBP rearrangements in acute myelogenous leukemia with t(8;16)
R H Giles, J G Dauwerse, C Higgins, et al.
American Journal of Human Genetics
|
October 27, 1997
A spectrum of mutations in the second gene for autosomal dominant polycystic kidney disease (PKD2)
B Veldhuisen, J J Saris, S de Haij, et al.
Clinical Genetics
|
May 22, 2010
X-chromosome duplications in males with mental retardation: pathogenic or benign variants?
A C J Gijsbers, N S den Hollander, A T J M Helderman-van de Enden, et al.
Neurobiology of Disease
|
October 21, 1999
Targeted disruption of the Cln3 gene provides a mouse model for Batten disease. The Batten Mouse Model Consortium [corrected]
H M Mitchison, D J Bernard, N D Greene, et al.
Kidney International
|
April 12, 2000
Location of mutations within the PKD2 gene influences clinical outcome
N Hateboer, B Veldhuisen, D Peters, et al.
Leukemia
|
September 1, 1996
Simple method for detection of MYH11 DNA rearrangements in patients with inv(16)(p13q22) and acute myeloid leukemia
B A van der Reijden, D Martinet, J G Dauwerse, et al.
Familial Cancer
|
October 24, 2003
Bannayan-Riley-Ruvalcaba syndrome: further delineation of the phenotype and management of PTEN mutation-positive cases
Y M C Hendriks, J T C M Verhallen, J J van der Smagt, et al.
Journal of Medical Genetics
|
June 14, 2008
Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant
F D Hannes, A J Sharp, H C Mefford, et al.
Page
of 17