Publication

Filipovic-Sadic S, Sah S, Chen L, Krosting J, Sekinger E, Zhang W, Hagerman PJ, Stenzel TT, Hadd AG, Latham GJ, Tassone F, A novel FMR1 PCR method for the routine detection of low abundance expanded alleles and full mutations in fragile X syndrome Clinical chemistry56:399-408 2010
PubMed ID: 20056738

Records Return:  (4) Show
 
Catalog IDGenderAge at SamplingFamilyRelationshipDescription
GM07541Female37 YR971maternal cousinFRAGILE X MENTAL RETARDATION SYNDROME
GM06891Male29 YR971brotherFRAGILE X MENTAL RETARDATION SYNDROME
GM20239Female42 YR probandFRAGILE X MENTAL RETARDATION SYNDROME
GM20230Male32 YR probandFRAGILE X MENTAL RETARDATION SYNDROME