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Journal of Genetic Counseling|July 5, 2015
Complex Genetic Disorders: Evaluating When Genetic Research Findings Are Applicable for Genetic Counseling PracticeC M Wolpert, E C Melvin, M C SpeerNeurosurgical Focus|May 9, 2006
A genetic hypothesis for Chiari I malformation with or without syringomyeliaM C Speer, T M George, D S Enterline, et al.Child Psychiatry and Human Development|October 18, 2005
The relationship between restrictive and repetitive behaviors in individuals with autism and obsessive compulsive symptoms in parentsR K Abramson, S A Ravan, H H Wright, et al.American Journal of Medical Genetics|July 18, 2000
Female with autistic disorder and monosomy X (Turner syndrome): parent-of-origin effect of the X chromosomeS L Donnelly, C M Wolpert, M M Menold, et al.American Journal of Medical Genetics|May 16, 2001
De novo partial duplication of chromosome 7p in a male with autistic disorderC M Wolpert, S L Donnelly, M L Cuccaro, et al.American Journal of Medical Genetics|August 14, 1995
Confirmation of locus heterogeneity in the pure form of familial spastic paraplegiaM C Speer, H M Kingston, R M Boustany, et al.American Journal of Medical Genetics|July 18, 2000
Three probands with autistic disorder and isodicentric chromosome 15C M Wolpert, M M Menold, M P Bass, et al.Journal of Neurogenetics|July 3, 2002
Association analysis of chromosome 15 gabaa receptor subunit genes in autistic disorderM M Menold, Y Shao, C M Wolpert, et al.Neurogenetics|March 25, 2000
Confirmation of a second locus for CMT2 and evidence for additional genetic heterogeneityM A Pericak-Vance, M C Speer, F Lennon, et al.Neurogenetics|September 13, 2000
Genetic studies in autistic disorder and chromosome 15M P Bass, M M Menold, C M Wolpert, et al.Pageof 2