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European Journal of Medical Genetics
|
September 11, 2016
Do the exome: A case of Williams-Beuren syndrome with severe epilepsy due to a truncating de novo variant in GABRA1
Bernt Popp, Regina Trollmann, Christian Büttner, et al.
BMC Musculoskeletal Disorders
|
November 22, 2019
Camptocormia as the presenting symptom in sporadic late onset nemaline myopathy: a case report
Matthias Türk, Armin M Nagel, Frank Roemer, et al.
American Journal of Medical Genetics. Part A
|
May 14, 2011
The smallest teeth in the world are caused by mutations in the PCNT gene
Piranit Kantaputra, Pranoot Tanpaiboon, Thantrira Porntaveetus, et al.
Human Brain Mapping
|
July 27, 2000
Effect of pentobarbital on visual processing in man
E Martin, T Thiel, P Joeri, et al.
Photosynthesis Research
|
October 18, 2005
An overview of the genome of Nostoc punctiforme, a multicellular, symbiotic cyanobacterium
J C Meeks, J Elhai, T Thiel, et al.
AJNR. American Journal of Neuroradiology
|
May 5, 2001
Lhermitte-Duclos disease: assessment with MR imaging, positron emission tomography, single-photon emission CT, and MR spectroscopy
J Klisch, F Juengling, J Spreer, et al.
Molecular Genetics and Genomics : MGG
|
August 26, 2003
Snipping polymorphisms from large EST collections in barley (Hordeum vulgare L.)
R Kota, S Rudd, A Facius, et al.
Molecular Genetics and Metabolism
|
July 6, 2004
Guanidinoacetate methyltransferase deficiency: differences of creatine uptake in human brain and muscle
R Ensenauer, T Thiel, K O Schwab, et al.
European Journal of Human Genetics : EJHG
|
November 22, 2017
Exome Pool-Seq in neurodevelopmental disorders
Bernt Popp, Arif B Ekici, Christian T Thiel, et al.
Cardiovascular and Interventional Radiology
|
November 1, 1996
Local intraarterial thrombolysis: in vitro comparison between automatic and manual pulse-spray infusion
J J Froelich, C Freymann, M Hoppe, et al.
Page
of 15
Search research articles
Search
Showing results (71-80 of 143) with videos related to
Sort By:
Page
of 15
European Journal of Medical Genetics
|
September 11, 2016
Do the exome: A case of Williams-Beuren syndrome with severe epilepsy due to a truncating de novo variant in GABRA1
Bernt Popp, Regina Trollmann, Christian Büttner, et al.
BMC Musculoskeletal Disorders
|
November 22, 2019
Camptocormia as the presenting symptom in sporadic late onset nemaline myopathy: a case report
Matthias Türk, Armin M Nagel, Frank Roemer, et al.
American Journal of Medical Genetics. Part A
|
May 14, 2011
The smallest teeth in the world are caused by mutations in the PCNT gene
Piranit Kantaputra, Pranoot Tanpaiboon, Thantrira Porntaveetus, et al.
Human Brain Mapping
|
July 27, 2000
Effect of pentobarbital on visual processing in man
E Martin, T Thiel, P Joeri, et al.
Photosynthesis Research
|
October 18, 2005
An overview of the genome of Nostoc punctiforme, a multicellular, symbiotic cyanobacterium
J C Meeks, J Elhai, T Thiel, et al.
AJNR. American Journal of Neuroradiology
|
May 5, 2001
Lhermitte-Duclos disease: assessment with MR imaging, positron emission tomography, single-photon emission CT, and MR spectroscopy
J Klisch, F Juengling, J Spreer, et al.
Molecular Genetics and Genomics : MGG
|
August 26, 2003
Snipping polymorphisms from large EST collections in barley (Hordeum vulgare L.)
R Kota, S Rudd, A Facius, et al.
Molecular Genetics and Metabolism
|
July 6, 2004
Guanidinoacetate methyltransferase deficiency: differences of creatine uptake in human brain and muscle
R Ensenauer, T Thiel, K O Schwab, et al.
European Journal of Human Genetics : EJHG
|
November 22, 2017
Exome Pool-Seq in neurodevelopmental disorders
Bernt Popp, Arif B Ekici, Christian T Thiel, et al.
Cardiovascular and Interventional Radiology
|
November 1, 1996
Local intraarterial thrombolysis: in vitro comparison between automatic and manual pulse-spray infusion
J J Froelich, C Freymann, M Hoppe, et al.
Page
of 15