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© 1991 Nature Publishing Group
© 1991 Nature Publishing Group
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Human genetics. Breaking the fragile X.
Notes on the population genetics of fragile X syndrome.
Fragile-X syndrome: unique genetics of the heritable unstable element.
Methylation analysis in newborn screening for fragile X syndrome--reply.
DNA methylation represses FMR-1 transcription in fragile X syndrome.
Fragile X-linked mental retardation and the difficulties of reverse genetics.
The fragile X syndrome.
The fragile X syndrome.
Population genetics of the fragile-X syndrome: multiallelic model for the FMR1 locus.
Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome.
ataxia syndrome.
Autism and fragile X syndrome.
Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome.
Fragile X spectrum disorders.
Genetics of human X-linked immunodeficiency diseases.
Fragile X syndrome.
Fragile X founder effect?
Fragile X mental retardation.
Fragile x premutation.
Fragile X syndrome.
Fragile X frequency.
Human pluripotent stem cell models of Fragile X syndrome.
ataxia syndrome: another phenotype of the fragile X gene.
Modeling Fragile X Syndrome Using Human Pluripotent Stem Cells.
Human genetics. Methylation and the fragile X.
© 1991 Nature Publishing Group © 1991 Nature Publishing Group...
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Recommend Documents
Human genetics. Breaking the fragile X.
Notes on the population genetics of fragile X syndrome.
Fragile-X syndrome: unique genetics of the heritable unstable element.
Methylation analysis in newborn screening for fragile X syndrome--reply.
DNA methylation represses FMR-1 transcription in fragile X syndrome.
Fragile X-linked mental retardation and the difficulties of reverse genetics.
The fragile X syndrome.
The fragile X syndrome.
Population genetics of the fragile-X syndrome: multiallelic model for the FMR1 locus.
Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome.
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