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Journal of Biomedical Materials Research
|
January 5, 2002
Novel current-conducting composite substrates for exposing osteoblasts to alternating current stimulation
P R Supronowicz, P M Ajayan, K R Ullmann, et al.
Clinical Genetics
|
October 19, 2007
Interstitial deletion of chromosome 4p associated with mild mental retardation, epilepsy and polymicrogyria of the left temporal lobe
R S Møller, C P Hansen, G D Jackson, et al.
American Journal of Medical Genetics. Part A
|
August 9, 2008
Investigation of 4q-deletion in two unrelated patients using array CGH
S S Kaalund, R S Møller, A Tészás, et al.
Stem Cell Research
|
November 25, 2023
Generation of two iPSC lines (MHHi001-A-12 and MHHi001-A-13) carrying biallelic truncating mutations at the 3'-end of SRCAP using CRISPR/Cas9
J Rhode, L Hagenau, J Beimdiek, et al.
The Journal of Pathology
|
November 5, 2003
Is high-grade adenomatous hyperplasia an early bronchioloalveolar adenocarcinoma?
R Ullmann, M Bongiovanni, I Halbwedl, et al.
Cytogenetic and Genome Research
|
September 16, 2006
Characterization of a de novo complex chromosome rearrangement (CCR) involving chromosomes 2 and 12, associated with mental retardation and impaired speech development
T Schwarzbraun, R Ullmann, M Schubert, et al.
Clinical Genetics
|
May 1, 2008
Mowat-Wilson syndrome: an underdiagnosed syndrome?
E Engenheiro, R S Møller, M Pinto, et al.
Kidney International
|
August 17, 2006
A complex phenotype with cystic renal disease
D Müller, E Klopocki, L M Neumann, et al.
Cytogenetic and Genome Research
|
December 28, 2007
Two independent chromosomal rearrangements, a very small (550 kb) duplication of the 7q subtelomeric region and an atypical 17q11.2 (NF1) microdeletion, in a girl with neurofibromatosis
O Bartsch, Z Vlcková, F Erdogan, et al.
Human Mutation
|
June 16, 2005
Novel rearrangement of chromosome band 22q11.2 causing 22q11 microdeletion syndrome-like phenotype and rhabdoid tumor of the kidney
R Wieser, B Fritz, R Ullmann, et al.
Page
of 7
Search research articles
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Showing results (51-60 of 67) with videos related to
Sort By:
Page
of 7
Journal of Biomedical Materials Research
|
January 5, 2002
Novel current-conducting composite substrates for exposing osteoblasts to alternating current stimulation
P R Supronowicz, P M Ajayan, K R Ullmann, et al.
Clinical Genetics
|
October 19, 2007
Interstitial deletion of chromosome 4p associated with mild mental retardation, epilepsy and polymicrogyria of the left temporal lobe
R S Møller, C P Hansen, G D Jackson, et al.
American Journal of Medical Genetics. Part A
|
August 9, 2008
Investigation of 4q-deletion in two unrelated patients using array CGH
S S Kaalund, R S Møller, A Tészás, et al.
Stem Cell Research
|
November 25, 2023
Generation of two iPSC lines (MHHi001-A-12 and MHHi001-A-13) carrying biallelic truncating mutations at the 3'-end of SRCAP using CRISPR/Cas9
J Rhode, L Hagenau, J Beimdiek, et al.
The Journal of Pathology
|
November 5, 2003
Is high-grade adenomatous hyperplasia an early bronchioloalveolar adenocarcinoma?
R Ullmann, M Bongiovanni, I Halbwedl, et al.
Cytogenetic and Genome Research
|
September 16, 2006
Characterization of a de novo complex chromosome rearrangement (CCR) involving chromosomes 2 and 12, associated with mental retardation and impaired speech development
T Schwarzbraun, R Ullmann, M Schubert, et al.
Clinical Genetics
|
May 1, 2008
Mowat-Wilson syndrome: an underdiagnosed syndrome?
E Engenheiro, R S Møller, M Pinto, et al.
Kidney International
|
August 17, 2006
A complex phenotype with cystic renal disease
D Müller, E Klopocki, L M Neumann, et al.
Cytogenetic and Genome Research
|
December 28, 2007
Two independent chromosomal rearrangements, a very small (550 kb) duplication of the 7q subtelomeric region and an atypical 17q11.2 (NF1) microdeletion, in a girl with neurofibromatosis
O Bartsch, Z Vlcková, F Erdogan, et al.
Human Mutation
|
June 16, 2005
Novel rearrangement of chromosome band 22q11.2 causing 22q11 microdeletion syndrome-like phenotype and rhabdoid tumor of the kidney
R Wieser, B Fritz, R Ullmann, et al.
Page
of 7