Showing results (41-50 of 3,648) with videos related to
Sort By:
Pageof 365
American Journal of Medical Genetics. Part A|March 26, 2003
Relationship of deficits of FMR1 gene specific protein with physical phenotype of fragile X males and females in pedigrees: a new perspectiveD Z Loesch, R M Huggins, Q M Bui, et al.American Journal of Medical Genetics|September 20, 2000
Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNAF Tassone, R J Hagerman, D Z Loesch, et al.American Journal of Medical Genetics|June 1, 1987
Phenotypic variation in male-transmitted fragile X: genetic inferencesD Z Loesch, D A Hay, G R Sutherland, et al.American Journal of Human Genetics|November 1, 1993
Genotype-phenotype relationships in fragile X syndrome: a family studyD Z Loesch, R Huggins, D A Hay, et al.Clinical Genetics|April 12, 2011
Fragile X-associated tremor/ataxia phenotype in a male carrier of unmethylated full mutation in the FMR1 geneD Z Loesch, S Sherwell, G Kinsella, et al.Journal of Medical Genetics|December 7, 2007
A low symptomatic form of neurodegeneration in younger carriers of the FMR1 premutation, manifesting typical radiological changesD Z Loesch, M Cook, L Litewka, et al.American Journal of Medical Genetics|February 24, 2001
Melatonin profiles and sleep characteristics in boys with fragile X syndrome: a preliminary studyE L Gould, D Z Loesch, M J Martin, et al.American Journal of Medical Genetics. Part A|September 2, 2003
Effect of fragile X status categories and FMRP deficits on cognitive profiles estimated by robust pedigree analysisD Z Loesch, R M Huggins, Q M Bui, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 30, 2011
White matter changes in basis pontis in small expansion FMR1 allele carriers with parkinsonismD Z Loesch, K Kotschet, N Trost, et al.Genetic Epidemiology|April 20, 2004
Hierarchical Bayes model for random haplotype and family effects in the transmission of fragile-XR M Huggins, D Z Loesch, G Q Qian, et al.Pageof 365