Search research articles
Contact Us
Filters
Showing results (1-10 of 19) with videos related to
Page
of 2
Sort By:
Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry
|
May 21, 2013
Durable micropatterns obtained from dissipative structures in liquid crystals
N Mießen, J Strauß, A Hoischen, et al.
Clinical Genetics
|
November 3, 2017
Homozygous mutation in ELMO2 may cause Ramon syndrome
C Mehawej, A Hoischen, R A Farah, et al.
Der Orthopade
|
July 21, 2009
[Pain staging, gender, and rehabilitation outcome in chronic low back pain. A pilot study]
P Hampel, A Brunnberg, B Krohn-Grimberghe, et al.
Neurology
|
March 7, 2007
DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation
H Engels, A Brockschmidt, A Hoischen, et al.
The Journal of Pathology
|
January 10, 2006
Comprehensive genomic analysis of desmoplastic medulloblastomas: identification of novel amplified genes and separate evaluation of the different histological components
A Ehrbrecht, U Müller, M Wolter, et al.
Journal of Dental Research
|
April 23, 2013
Non-syndromic tooth agenesis associated with a nonsense mutation in ectodysplasin-A (EDA)
T Nikopensius, T Annilo, T Jagomägi, et al.
Clinical and Experimental Immunology
|
December 22, 2020
Mimicking Behçet's disease: GM-CSF gain of function mutation in a family suffering from a Behçet's disease-like disorder marked by extreme pathergy
B Rösler, B Heinhuis, X Wang, et al.
Molecular Syndromology
|
July 22, 2010
Severe Progressive Autism Associated with Two de novo Changes: A 2.6-Mb 2q31.1 Deletion and a Balanced t(14;21)(q21.1;p11.2) Translocation with Long-Range Epigenetic Silencing of LRFN5 Expression
D R H de Bruijn, A H A van Dijk, R Pfundt, et al.
Oncogene
|
August 11, 2010
Trisomic dose of several chromosome 21 genes perturbs haematopoietic stem and progenitor cell differentiation in Down's syndrome
S De Vita, C Canzonetta, C Mulligan, et al.
Journal of Internal Medicine
|
February 3, 2015
A missense mutation underlies defective SOCS4 function in a family with autoimmunity
P Arts, T S Plantinga, J M van den Berg, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 19) with videos related to
Sort By:
Page
of 2
Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry
|
May 21, 2013
Durable micropatterns obtained from dissipative structures in liquid crystals
N Mießen, J Strauß, A Hoischen, et al.
Clinical Genetics
|
November 3, 2017
Homozygous mutation in ELMO2 may cause Ramon syndrome
C Mehawej, A Hoischen, R A Farah, et al.
Der Orthopade
|
July 21, 2009
[Pain staging, gender, and rehabilitation outcome in chronic low back pain. A pilot study]
P Hampel, A Brunnberg, B Krohn-Grimberghe, et al.
Neurology
|
March 7, 2007
DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation
H Engels, A Brockschmidt, A Hoischen, et al.
The Journal of Pathology
|
January 10, 2006
Comprehensive genomic analysis of desmoplastic medulloblastomas: identification of novel amplified genes and separate evaluation of the different histological components
A Ehrbrecht, U Müller, M Wolter, et al.
Journal of Dental Research
|
April 23, 2013
Non-syndromic tooth agenesis associated with a nonsense mutation in ectodysplasin-A (EDA)
T Nikopensius, T Annilo, T Jagomägi, et al.
Clinical and Experimental Immunology
|
December 22, 2020
Mimicking Behçet's disease: GM-CSF gain of function mutation in a family suffering from a Behçet's disease-like disorder marked by extreme pathergy
B Rösler, B Heinhuis, X Wang, et al.
Molecular Syndromology
|
July 22, 2010
Severe Progressive Autism Associated with Two de novo Changes: A 2.6-Mb 2q31.1 Deletion and a Balanced t(14;21)(q21.1;p11.2) Translocation with Long-Range Epigenetic Silencing of LRFN5 Expression
D R H de Bruijn, A H A van Dijk, R Pfundt, et al.
Oncogene
|
August 11, 2010
Trisomic dose of several chromosome 21 genes perturbs haematopoietic stem and progenitor cell differentiation in Down's syndrome
S De Vita, C Canzonetta, C Mulligan, et al.
Journal of Internal Medicine
|
February 3, 2015
A missense mutation underlies defective SOCS4 function in a family with autoimmunity
P Arts, T S Plantinga, J M van den Berg, et al.
Page
of 2