Add to ORKGAll in-text references underlined in blue are linked to publications on ResearchGate, letting you access and read them immediately
Fragile X syndrome is an X-linked dominant disorder with incomplete penetrance that is a common caus...
The Fragile X-related disorders (FXDs), which include the intellectual disability fragile X syndrome...
Fragile X Syndrome (FXS) is a genetic disease due to a CGG trinucleotide expansion, named full muta...
All in-text references underlined in blue are linked to publications on ResearchGate, letting you ac...
All in-text references underlined in blue are linked to publications on ResearchGate, letting you ac...
Contains fulltext : mmubn000001_219285284.pdf (publisher's version ) (Open Access)...
Fragile X Syndrome (FXS) is a genetic disease due to a CGG trinucleotide expansion, named full mutat...
The fragile X mental retardation 1 gene located on the X-chromosome plays a role in protein synthesi...
More than 20 human hereditary diseases have been linked to expansions of unstable simple nucleotide ...
All in-text references underlined in blue are linked to publications on ResearchGate, letting you ac...
Fragile X Syndrome (FraX) is a commonly inherited mental retardation disorder causing hyperactivity,...
Fragile X Syndrome (FXS) is a genetic disease due to a CGG trinucleotide expansion, named full mutat...
Fragile X syndrome is the monogenetic condition that produces more cases of autism and intellectual ...
Fragile X Syndrome (FXS) is the most frequent hereditary form of mental retardation, caused by an ex...
César Payán-Gómez,1 Julian Ramirez-Cheyne,2,3 Wilmar Saldarriaga2,3 1Deparment of Biology, Faculty o...
Fragile X syndrome is an X-linked dominant disorder with incomplete penetrance that is a common caus...
The Fragile X-related disorders (FXDs), which include the intellectual disability fragile X syndrome...
Fragile X Syndrome (FXS) is a genetic disease due to a CGG trinucleotide expansion, named full muta...
All in-text references underlined in blue are linked to publications on ResearchGate, letting you ac...
All in-text references underlined in blue are linked to publications on ResearchGate, letting you ac...
Contains fulltext : mmubn000001_219285284.pdf (publisher's version ) (Open Access)...
Fragile X Syndrome (FXS) is a genetic disease due to a CGG trinucleotide expansion, named full mutat...
The fragile X mental retardation 1 gene located on the X-chromosome plays a role in protein synthesi...
More than 20 human hereditary diseases have been linked to expansions of unstable simple nucleotide ...
All in-text references underlined in blue are linked to publications on ResearchGate, letting you ac...
Fragile X Syndrome (FraX) is a commonly inherited mental retardation disorder causing hyperactivity,...
Fragile X Syndrome (FXS) is a genetic disease due to a CGG trinucleotide expansion, named full mutat...
Fragile X syndrome is the monogenetic condition that produces more cases of autism and intellectual ...
Fragile X Syndrome (FXS) is the most frequent hereditary form of mental retardation, caused by an ex...
César Payán-Gómez,1 Julian Ramirez-Cheyne,2,3 Wilmar Saldarriaga2,3 1Deparment of Biology, Faculty o...
Fragile X syndrome is an X-linked dominant disorder with incomplete penetrance that is a common caus...
The Fragile X-related disorders (FXDs), which include the intellectual disability fragile X syndrome...
Fragile X Syndrome (FXS) is a genetic disease due to a CGG trinucleotide expansion, named full muta...