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Annales De Chirurgie|March 24, 2005
[CT-Guided transgluteal approach for percutaneous drainage of pelvic abscesses: results in 21 patients]P Soyer, M Boudiaf, A Alves, et al.Journal of Neurology, Neurosurgery, and Psychiatry|May 18, 1999
Probability of bilateral disease in people presenting with a unilateral vestibular schwannomaD G Evans, R Lye, W Neary, et al.American Journal of Human Genetics|August 27, 1998
Somatic mosaicism: a common cause of classic disease in tumor-prone syndromes? Lessons from type 2 neurofibromatosisD G Evans, A J Wallace, C L Wu, et al.Nature|February 13, 1992
Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box geneM Tassabehji, A P Read, V E Newton, et al.Annales De L'Institut Pasteur. Immunologie|January 1, 1985
Allelism in the HLA class I multigene familyR Sodoyer, C Nguyen, T Strachan, et al.The Journal of Biological Chemistry|December 24, 2008
Ribosomal S6 kinase 2 directly phosphorylates the 5-hydroxytryptamine 2A (5-HT2A) serotonin receptor, thereby modulating 5-HT2A signalingRyan T Strachan, Douglas J Sheffler, Belinda Willard, et al.Nature Genetics|January 1, 1993
Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2M Tassabehji, A P Read, V E Newton, et al.Physiological Research|July 14, 2023
Association of selected inflammatory biomarkers with cough reflex sensitivity in asthmatic childrenP Kunč, J Fábry, M Grendár, et al.European Journal of Pediatrics|January 1, 1992
Metabolic pigmentary retinopathies: diagnosis and therapeutic attemptsB T Poll-The, T Billette de Villemeur, M Abitbol, et al.Nucleic Acids Research|March 11, 1990
Large restriction fragments containing poly-TG are highly polymorphic in a variety of vertebratesY Kashi, Y Tikochinsky, E Genislav, et al.Pageof 96