Rubinstein-Taybi syndrome: five cosmids should be used for microdeletion detection and low number of protein truncating mutation
Rubinstein-Taybi syndrome (RSTS) is a rare autosomal dominant disorder characterised by facial dysmo...
International audienceThe Rubinstein-Taybi syndrome (RSTS) is a rare congenital developmental disord...
The Rubinstein-Taybi syndrome (RSTS; OMIM #180849, #613684) is a rare developmental disorder charact...
Title Diagnostic analysis of th Rubinstein-Taybi syndrome: five cosmids should be used for microdele...
Review on Rubinstein-Taybi syndrome (RTS), with data on clinics, and the genes involved
International audienceBackground: Rubinstein-Taybi syndrome (RSTS; OMIM 180849) is a rare autosomal ...
Background: Rubinstein-Taybi Syndrome (RSTS, MIM 180849) is a rare congenital disorder characterized...
Rubinstein-Taybi syndrome (RSTS) is a rare congenital neurodevelopmental disorder characterized by p...
BackgroundRubinstein-Taybi syndrome (RSTS) is an extremely rare autosomal dominant genetic disease, ...
Rubinstein-Taybi syndrome (RSTS) is a rare, congenital, plurimalformative, and neurodevelopmental di...
<p>The aim of the article is to present clinical experience of studying the patient with a genetic s...
Rubinstein-Taybi syndrome (RSTS) is a developmental disorder characterized by a typical face and dis...
BACKGROUND Rubinstein-Taybi syndrome (RSTS) is a congenital disorder characterised by growth reta...
Rubinstein-Taybi syndrome (RSTS) is a rare autosomal dominant genetic disease and is characterized b...
The genetic basis of Rubinstein-Taybi syndrome (RSTS), a rare, sporadic, clinically heterogeneous di...
Rubinstein-Taybi syndrome (RSTS) is a rare autosomal dominant disorder characterised by facial dysmo...
International audienceThe Rubinstein-Taybi syndrome (RSTS) is a rare congenital developmental disord...
The Rubinstein-Taybi syndrome (RSTS; OMIM #180849, #613684) is a rare developmental disorder charact...
Title Diagnostic analysis of th Rubinstein-Taybi syndrome: five cosmids should be used for microdele...
Review on Rubinstein-Taybi syndrome (RTS), with data on clinics, and the genes involved
International audienceBackground: Rubinstein-Taybi syndrome (RSTS; OMIM 180849) is a rare autosomal ...
Background: Rubinstein-Taybi Syndrome (RSTS, MIM 180849) is a rare congenital disorder characterized...
Rubinstein-Taybi syndrome (RSTS) is a rare congenital neurodevelopmental disorder characterized by p...
BackgroundRubinstein-Taybi syndrome (RSTS) is an extremely rare autosomal dominant genetic disease, ...
Rubinstein-Taybi syndrome (RSTS) is a rare, congenital, plurimalformative, and neurodevelopmental di...
<p>The aim of the article is to present clinical experience of studying the patient with a genetic s...
Rubinstein-Taybi syndrome (RSTS) is a developmental disorder characterized by a typical face and dis...
BACKGROUND Rubinstein-Taybi syndrome (RSTS) is a congenital disorder characterised by growth reta...
Rubinstein-Taybi syndrome (RSTS) is a rare autosomal dominant genetic disease and is characterized b...
The genetic basis of Rubinstein-Taybi syndrome (RSTS), a rare, sporadic, clinically heterogeneous di...
Rubinstein-Taybi syndrome (RSTS) is a rare autosomal dominant disorder characterised by facial dysmo...
International audienceThe Rubinstein-Taybi syndrome (RSTS) is a rare congenital developmental disord...
The Rubinstein-Taybi syndrome (RSTS; OMIM #180849, #613684) is a rare developmental disorder charact...
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