共 50 条
- [41] A single nucleoticle variant in the FMR1 CGG repeat results in a "Pseudodeletion" and is not associated with the Fragile X syndrome phenotype JOURNAL OF MOLECULAR DIAGNOSTICS, 2008, 10 (03): : 272 - 275
- [42] The role of AGG interruptions in the FMR1 gene stability: A survey in ethnic groups with low and high rate of consanguinity MOLECULAR GENETICS & GENOMIC MEDICINE, 2019, 7 (10):
- [48] Validation of a Commercially Available Screening Tool for the Rapid Identification of CGG Trinucleotide Repeat Expansions in FMR1 JOURNAL OF MOLECULAR DIAGNOSTICS, 2015, 17 (03): : 302 - 314
- [50] Examination of the Effect of the Polymorphic CGG Repeat in the FMR1 Gene on Cognitive Performance Behavior Genetics, 2005, 35 : 435 - 445