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Annals of Neurology|October 1, 1986
X-linked neuropathy: gene localization with DNA probesK H Fischbeck, N ar-Rushdi, M Pericak-Vance, et al.Helvetica Paediatrica Acta|November 1, 1988
Trisomy 3q2 and Pierre-Robin sequence in a boy with unbalanced 46,XY, der(10), t(3;10)(q23;q26.3) de novo karyotypeA Kleczkowska, J P Fryns, F Moerman, et al.Journal of Pediatric Psychology|May 20, 1998
Problem behaviors and personality of children and adolescents with Prader-Willi syndromeC F van Lieshout, R E de Meyer, L M Curfs, et al.Cytogenetic and Genome Research|March 9, 2004
A physical map of the chromosome 12 centromereJ R Vermeesch, H Duhamel, P Raeymaekers, et al.Human Genetics|April 1, 1997
Molecular analysis of the beta-glucuronidase gene: novel mutations in mucopolysaccharidosis type VII and heterogeneity of the polyadenylation regionR Vervoort, N R Buist, W J Kleijer, et al.Clinical Genetics|March 1, 1984
Anomalous cerebral venous drainage in Aarskog syndromeP van den Bergh, J P Fryns, G Wilms, et al.Clinical Genetics|June 1, 1991
A clinical, cytogenetic and familial study of 307 mentally retarded, institutionalized, adult male patients with special interest for fra(X) negative X-linked mental retardationM Haspeslagh, J P Fryns, M Holvoet, et al.The European Respiratory Journal|June 11, 1999
Systemic lupus erythematosus, eosinophilia and Löffler's endocarditis. An unusual associationM Thomeer, P Moerman, R Westhovens, et al.Urologia Internationalis|January 1, 1988
Benign mesothelioma of the epididymis: case reportH Van Poppel, K Van Renterghem, H Claes, et al.European Journal of Pediatrics|December 1, 1984
The Coffin-Lowry syndrome. A study of two new index patients and their familiesM Haspeslagh, J P Fryns, L Beusen, et al.Pageof 89