论文信息 - Expanding the phenotype of ASXL3‐related syndrome: A comprehensive description of 45 unpublished individuals with inherited and de novo pathogenic variants in ASXL3 - 字舞流文

Expanding the phenotype of ASXL3‐related syndrome: A comprehensive description of 45 unpublished individuals with inherited and de novo pathogenic variants in ASXL3

J. Graham | F. Alkuraya | N. Hauser | R. Harrison | R. Newbury-Ecob | B. Cogné | U. Kini | A. Slavotinek | B. Isidor | E. Reid | Arjan Bouman | Diana S. Johnson | S. Lynch | M. Willemsen | P. Prontera | R. Armstrong | M. Balasubramanian | A. Dixit | R. Fisher | N. Ragge | J. Vogt | C. Cunniff | T. Challman | P. Blanchet | Dong Li | C. Ockeloen | S. Demirdas | N. Meeks | Y. Si | A. Bruel | J. Pappas | J. Cohen | Deanna Alexis Carere | Emily Palen | J. Walia | R. Rabin | S. Naik | S. S. Schrier Vergano | D. A. Carere | D. Renaud | Schaida Schirwani | N. Foulds | M. J. Guillen Sacoto | Katheryn L. Grand | J. Dean | Valerie Slegesky | Natalie Dykzeul | S. Albaba | M. Tedesco | Rachel E. Harrison | Katherine Bergstrom | Francisca Milan Zamora | Dayna Morel | Hessa F. Albassam | Costa Cinzia | Paula Girotto | Julie S. Cohen