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Wiener Klinische Wochenschrift|January 1, 1996
Intensive care management of acute pancreatitis: recognition of patients at high risk of developing severe or fatal complicationsP Kaufmann, G Hofmann, K H Smolle, et al.
Genetic Counseling (Geneva, Switzerland)|November 15, 2006
Multiple congenital abnormalities in a newborn with two supernumerary marker chromosomes derived from chromosome 14B H W Faas, J Van Der Deure, M I Wunderink, et al.
Brain Research. Developmental Brain Research|July 6, 2005
Nucleotide variation analysis does not support a causal role for plexin-A1 in hereditary congenital facial paresisBert van der Zwaag, J Peter H Burbach, Han G Brunner, et al.
Muscle & Nerve|March 1, 1992
Eye movement disorder: an early expression of the myotonic dystrophy gene?J P ter Bruggen, C C Tijssen, H G Brunner, et al.
Psychopathology|November 27, 2009
Psychiatric profile in rubinstein-taybi syndrome. A review and case reportW M A Verhoeven, S Tuinier, H J H Kuijpers, et al.
Journal of Medical Genetics|October 23, 1998
The prevalence of PAX2 mutations in patients with isolated colobomas or colobomas associated with urogenital anomaliesH E Cunliffe, L A McNoe, T A Ward, et al.
European Journal of Human Genetics : EJHG|August 10, 2006
A novel CSX/NKX2-5 mutation causes autosomal-dominant AV block: are atrial fibrillation and syncopes part of the phenotype?Ilse Gutierrez-Roelens, Luc De Roy, Caroline Ovaert, et al.
Anticancer Research|September 1, 1996
Inhibition of glycosylphosphatidylinositol (GPI) phospholipase D by suramin-like compoundsG Brunner, L Zalkow, E Burgess, et al.
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