Expanding the phenotype of
ASXL3
‐related syndrome: A comprehensive description of 45 unpublished individuals with inherited and de novo pathogenic variants in
ASXL3
Schaida Schirwani , Shadi Albaba , Deanna Alexis Carere , Maria J. Guillen Sacoto , Francisca Milan Zamora , Yue Si , Rachel Rabin , John Pappas , Deborah L. Renaud , Natalie Hauser , Evan Reid , Patricia Blanchet , Nichola Foulds , Abhijit Dixit , Richard Fisher , Ruth Armstrong , Bertrand Isidor , Benjamin Cogne , Samantha Schrier Vergano , Serwet Demirdas , Natalie Dykzeul , Julie S. Cohen , Katheryn Grand , Dayna Morel , Anne Slavotinek , Hessa F. Albassam , Swati Naik , John Dean , Nicola Ragge , Costa Cinzia , Maria Giovanna Tedesco , Rachel E. Harrison , Arjan Bouman , Emily Palen , Thomas D. Challman , Marjolein H. Willemsen , Julie Vogt , Christopher Cunniff , Katherine Bergstrom , Jagdeep S. Walia , Ange‐Line Bruel , Usha Kini , Fowzan S. Alkuraya , Valerie Slegesky , Naomi Meeks , Paula Girotto , Diana Johnson , Ruth Newbury‐Ecob , Charlotte W. Ockeloen , Paolo Prontera , Sally Ann Lynch , Dong Li , John M. Graham , Meena Balasubramanian American Journal of Medical Genetics Part A(2021)
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