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American Journal of Medical Genetics|April 27, 2002
No evidence for submicroscopic 22qter deletions in patients with features suggestive for Angelman syndromeBert B A de Vries, Jess Tyson, Robin M Winter, et al.Neuropediatrics|February 1, 1994
Disordered peripheral nerve conduction in DOOR(S) syndromeW Reardon, S Boyd, M C Pitt, et al.Chemistry and Physics of Lipids|November 1, 1996
Anesthetics modulate phospholipase C hydrolysis of monolayer phospholipids by surface pressureD M Goodman, E M Nemoto, R W Evans, et al.International Journal of Cancer|July 15, 1994
DNA repair capacity as a risk factor for non-melanocytic skin cancer--a molecular epidemiological studyJ Hall, D R English, M Artuso, et al.Gastroenterology|July 1, 1994
Structural and functional adaptation following jejunal resection in rabbits: effect of epidermal growth factorE O'Loughlin, M Winter, A Shun, et al.Journal of Medical Genetics|April 1, 1996
The dysmorphic human-mouse homology database (DHMHD): an interactive World-Wide Web resource for gene mappingC D Evans, A G Searle, A A Schinzel, et al.Anesthesia and Analgesia|August 1, 1996
In vivo imaging of human limbic responses to nitrous oxide inhalationF E Gyulai, L L Firestone, M A Mintun, et al.Clinical Dysmorphology|April 1, 1996
Serpentine fibula syndrome: expansion of the phenotype with three affected siblingsE M Rosser, N P Mann, C M Hall, et al.Stroke|April 1, 1996
Effect of time and cerebrovascular symptoms of the prevalence of microembolic signals in patients with cervical carotid stenosisA M Forteza, V L Babikian, C Hyde, et al.Human Molecular Genetics|August 1, 1997
The TWIST gene, although not disrupted in Saethre-Chotzen patients with apparently balanced translocations of 7p21, is mutated in familial and sporadic casesC S Rose, P Patel, W Reardon, et al.Pageof 129