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high-performance liquid chromatographyTopical concept
Through the use of post-PCR high-performance liquid chromatography, 65 percent of 20 RS patients were found to have mutation(s) in the MECP2
AbstractRett syndrome (RTT) is a progressive neurodevelopmental disorder that affects mainly females...
Comprehensive genetic screening programs have led to the identification of pathogenic methyl-CpG-bin...
Rett syndrome is an X-linked dominant neurological disorder, which appears to be the commonest genet...
MECP2 mutations are identifiable in ∼80% of classic Rett syndrome (RTT), but less frequently in atyp...
MECP2 mutations are identifiable in ∼80% of classic Rett syndrome (RTT), but less frequently in atyp...
Abstract Background Rett syndrome (RTT) is a severe neurodevelopmental disorder in children characte...
Rett syndrome (RTT) is a progressive neurodevelopmental disorder that is caused by mutations in the ...
Background Classical Rett syndrome is a severe neurodevelopmental X-linked dominant disorder affecti...
EPM UNIFESP, Ctr Genet Med, Sao Paulo, BrazilUniv Sao Paulo, Dept Biol IB, Sao Paulo, BrazilUniv Sao...
Seventy-one sporadic and 7 familial Rett syndrome (RTT) patients were screened for MECP2 mutations b...
Rett syndrome is a progressive neurodevelopmental disorder occurring predominantly in females. Recen...
Aim: This study aimed to characterize MECP2 gene variants in Indian female patients with classical R...
MECP2 mutations are identifiable in,80 % of classic Rett syndrome (RTT), but less frequently in atyp...
Mutations in the methyl-CpG-binding protein gene MECP2 at Xq28 cause Rett syndrome (RTT), an X-linke...
Rett Syndrome (RTT) is an X-linked dominant neurodevelopmental disorder, which almost exclusively af...
AbstractRett syndrome (RTT) is a progressive neurodevelopmental disorder that affects mainly females...
Comprehensive genetic screening programs have led to the identification of pathogenic methyl-CpG-bin...
Rett syndrome is an X-linked dominant neurological disorder, which appears to be the commonest genet...
MECP2 mutations are identifiable in ∼80% of classic Rett syndrome (RTT), but less frequently in atyp...
MECP2 mutations are identifiable in ∼80% of classic Rett syndrome (RTT), but less frequently in atyp...
Abstract Background Rett syndrome (RTT) is a severe neurodevelopmental disorder in children characte...
Rett syndrome (RTT) is a progressive neurodevelopmental disorder that is caused by mutations in the ...
Background Classical Rett syndrome is a severe neurodevelopmental X-linked dominant disorder affecti...
EPM UNIFESP, Ctr Genet Med, Sao Paulo, BrazilUniv Sao Paulo, Dept Biol IB, Sao Paulo, BrazilUniv Sao...
Seventy-one sporadic and 7 familial Rett syndrome (RTT) patients were screened for MECP2 mutations b...
Rett syndrome is a progressive neurodevelopmental disorder occurring predominantly in females. Recen...
Aim: This study aimed to characterize MECP2 gene variants in Indian female patients with classical R...
MECP2 mutations are identifiable in,80 % of classic Rett syndrome (RTT), but less frequently in atyp...
Mutations in the methyl-CpG-binding protein gene MECP2 at Xq28 cause Rett syndrome (RTT), an X-linke...
Rett Syndrome (RTT) is an X-linked dominant neurodevelopmental disorder, which almost exclusively af...
AbstractRett syndrome (RTT) is a progressive neurodevelopmental disorder that affects mainly females...
Comprehensive genetic screening programs have led to the identification of pathogenic methyl-CpG-bin...
Rett syndrome is an X-linked dominant neurological disorder, which appears to be the commonest genet...
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