Publication

Verkerk AJ, Pieretti M, Sutcliffe JS, Fu YH, Kuhl DP, Pizzuti A, Reiner O, Richards S, Victoria MF, Zhang FP, et al, Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell65:905-14 1991
PubMed ID: 1710175

Records Return:  (5) Show
 
Catalog IDGenderAge at SamplingFamilyRelationshipDescription
GM06897Male25 YR971probandFRAGILE X MENTAL RETARDATION SYNDROME
GM06912Male17 YR970probandFRAGILE X MENTAL RETARDATION SYNDROME
GM04025Male29 YR588probandFRAGILE X MENTAL RETARDATION SYNDROME
GM07294Male33 YR1011probandFRAGILE X MENTAL RETARDATION SYNDROME
GM03200Male34 YR probandFRAGILE X MENTAL RETARDATION SYNDROME