Informação

RAD21


RAD21 also forms part of the core cohesin complex. Changes in RAD21 have been found in a small percentage (1-2%) of causes for CdLS. Individuals with changes in RAD21 are reported to have a non-classic CdLS phenotype.


                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                              

Encontrar outras páginas que partilhem o mesmo tópico que esta página O que é a Síndrome de Cornelia de Lange (SCdL)?2

                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                              

tópico que contém este tópico
Moleculair diagnostic criteria
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Informação

  

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