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American Journal of Medical Genetics|February 1, 1991
Cytogenetically negative, linkage positive "fragile X" syndromeS Sklower Brooks, I Cohen, C Ferrando, et al.
Human Genetics|June 30, 1977
De novo trisomy 9pter leads to q13N B Kardon, H R Salwen, M A Krauss, et al.
American Journal of Medical Genetics|February 1, 1991
Linkage in fragile X families of three distal flanking markers: ST14, DX13, and F8W T Brown, A C Gross, P Goonewardena, et al.
Human Genetics|June 30, 1977
A case of 46,XY,t(1;13) (q24;q32) with mental retardationL Wilbur, F M Curcuru-Giordano, S G Krishna, et al.
Genetic Testing|September 12, 2001
PCR-based methylation testing for Prader-Willi or Angelman syndromes using archived fixed-cell suspensionsM Velinov, H Gu, K Shah, et al.
Alzheimer Disease and Associated Disorders|January 1, 1990
Study of spindle microtubule reassembly in cells from Alzheimer and Down syndrome patients following exposure to colcemidM S Krawczun, E C Jenkins, K P Lele, et al.
American Journal of Human Genetics|January 1, 1985
Chromosomal localization of several families of repetitive sequences by in situ hybridizationE A Devine, S L Nolin, G E Houck, et al.
American Journal of Human Genetics|February 1, 1991
Why are autism and the fragile-X syndrome associated? Conceptual and methodological issuesI L Cohen, V Sudhalter, A Pfadt, et al.
Annales De Genetique|June 9, 2004
Characterization of an analphoid, neocentromere-positive inv dup 8p marker chromosome using multiplex whole chromosome and sub-telomere FISH analysesM Velinov, H Gu, M Genovese, et al.
American Journal of Medical Genetics|April 18, 1997
Longer brainstem auditory evoked response latencies of individuals with fragile X syndrome related to sedationC M Miezejeski, G Heaney, R Belser, et al.
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