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American Journal of Medical Genetics|March 1, 1992
Absent thumb, immune disorder, and congenital anemia presenting with hydrops fetalisB A Semmekrot, A Haraldsson, C M Weemaes, et al.The Journal of Pediatrics|December 10, 1999
Patterns of cognitive functioning in school-aged children with Noonan syndrome associated with variability in phenotypic expressionI van der Burgt, G Thoonen, N Roosenboom, et al.European Journal of Human Genetics : EJHG|January 17, 2003
A new web-based data mining tool for the identification of candidate genes for human genetic disordersMarc A van Driel, Koen Cuelenaere, Patrick P C W Kemmeren, et al.Neurology|January 1, 1991
Genetic linkage with chromosome 19 but not chromosome 17 in a family with myotonic dystrophy associated with hereditary motor and sensory neuropathyH G Brunner, F Spaans, H J Smeets, et al.American Journal of Medical Genetics|June 1, 1993
Exclusion of the neurofibromatosis 1 locus in a family with inherited café-au-lait spotsH G Brunner, T Hulsebos, P M Steijlen, et al.The American Journal of Psychiatry|July 7, 2011
Association of the Alzheimer's gene SORL1 with hippocampal volume in young, healthy adultsJanita Bralten, Alejandro Arias-Vásquez, Remco Makkinje, et al.Journal of Medical Genetics|November 1, 1992
Presymptomatic diagnosis of myotonic dystrophyH G Brunner, W Nillesen, B A van Oost, et al.Human Molecular Genetics|September 1, 1994
A Stickler syndrome gene is linked to chromosome 6 near the COL11A2 geneH G Brunner, S E van Beersum, M L Warman, et al.American Journal of Medical Genetics|June 13, 1997
Oto- spondylo-megaepiphyseal dysplasia (OSMED): clinical description of three patients homozygous for a missense mutation in the COL11A2 geneM A van Steensel, P Buma, M C de Waal Malefijt, et al.Journal of Natural Products|April 1, 1997
The secalosides, novel tumor cell growth inhibitory glycosides from a pollen extractJ C Jaton, K Roulin, K Rose, et al.Pageof 63