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Clinical Genetics|August 1, 1984
Mosaic tetrasomy 21 in a male childM L Kwee, P G Barth, F Arwert, et al.
Brain & Development|January 1, 1982
Familial lissencephaly with extreme neopallial hypoplasiaP G Barth, R Mullaart, F C Stam, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 4, 2000
Subependymal nodular heterotopia in patients with encephaloceleF A Roelens, P G Barth, J J van der Harten
Neuropediatrics|June 21, 2002
"Vanishing white matter" and ovarian dysgenesis in an infant with cerebro-oculo-facio-skeletal phenotypeE Boltshauser, P G Barth, D Troost, et al.
Journal of Comparative Physiology. A, Neuroethology, Sensory, Neural, and Behavioral Physiology|August 10, 2006
Arthropod mechanoreceptive hairs: modeling the directionality of the jointHans-Erich Dechant, Bernhard Hössl, Franz G Rammerstorfer, et al.
Journal of Comparative Physiology. A, Neuroethology, Sensory, Neural, and Behavioral Physiology|December 23, 2006
Finite element modeling of arachnid slit sensilla-I. The mechanical significance of different slit arraysBernhard Hössl, Helmut J Böhm, Franz G Rammerstorfer, et al.
Acta Neuropathologica|April 26, 1978
Tuberous sclerosis and dysplasia of the corpus callosum. Case report of their combined occurrence in a newbornP G Barth, F C Stam, J J von der Harten
Child'S Brain|January 1, 1981
Congenital multiple angiomatosis with brain involvementL M Smit, P G Barth, F C Stam, et al.
Yeast (Chichester, England)|November 26, 1999
trans-dominant mutations in the GPR1 gene cause high sensitivity to acetic acid and ethanol in the yeast Yarrowia lipolyticaK Tzschoppe, A Augstein, R Bauer, et al.
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