Aortic root dilatation and dilated cardiomyopathy in an adult with Tatton‐Brown‐Rahman syndrome
Abstract Tatton‐Brown‐Rahman syndrome is an autosomal dominant overgrowth syndrome
caused by pathogenic DNMT3A variants in the germline. Clinical findings of tall stature due …
caused by pathogenic DNMT3A variants in the germline. Clinical findings of tall stature due …
Aortic root dilatation and dilated cardiomyopathy in an adult with Tatton-Brown-Rahman syndrome.
AC Cecchi, A Haidar, I Marin, CS Kwartler… - American Journal of …, 2021 - europepmc.org
Abstract Tatton-Brown-Rahman syndrome is an autosomal dominant overgrowth syndrome
caused by pathogenic DNMT3A variants in the germline. Clinical findings of tall stature due …
caused by pathogenic DNMT3A variants in the germline. Clinical findings of tall stature due …
[HTML][HTML] Aortic Root Dilatation and Dilated Cardiomyopathy in an Adult with Tatton-Brown-Rahman Syndrome
AC Cecchi, A Haidar, I Marin, CS Kwartler… - American journal of …, 2022 - ncbi.nlm.nih.gov
Abstract Tatton-Brown-Rahman syndrome is an autosomal dominant overgrowth syndrome
caused by pathogenic DNMT3A variants in the germline. Clinical findings of tall stature due …
caused by pathogenic DNMT3A variants in the germline. Clinical findings of tall stature due …
Aortic root dilatation and dilated cardiomyopathy in an adult with Tatton-Brown-Rahman syndrome
AC Cecchi, A Haidar, I Marin… - … journal of medical …, 2022 - pubmed.ncbi.nlm.nih.gov
Tatton-Brown-Rahman syndrome is an autosomal dominant overgrowth syndrome caused
by pathogenic DNMT3A variants in the germline. Clinical findings of tall stature due to …
by pathogenic DNMT3A variants in the germline. Clinical findings of tall stature due to …