Search Results - "Iber, J C"

Characterization of the full fragile X syndrome mutation in fetal gametes by Malter, Henry E, Iber, Jane C, Willemsen, R, Graaff, Esther de, Tarleton, Jack C, Leisti, J, Warren, Stephen T, Oostra, Ben A

“…Fragile X syndrome results from the expansion of the CGG repeat in the FMR1 gene. Expansion has been suggested to be a postzygotic event with the germline…”
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The effect of FMR1 CGG repeat interruptions on mutation frequency as measured by sperm typing by Kunst, C B, Leeflang, E P, Iber, J C, Arnheim, N, Warren, S T

“…Fragile X syndrome results from the unstable expansion of a CGG repeat within the FMR1 gene. Three classes of FMR1 alleles have been identified, normal alleles…”
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