Expanding the Phenotype of ASXL3-related Syndrome: a Comprehensive Description of 45 Unpublished Individuals with Inherited and De Novo Pathogenic Variants in ASXL3 (vol 185A, Pg 3446, 2021) Schaida Schirwani , Albaba J. Shadi , Deanna Alexis Carere ,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 , Cinzia Costa , 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 , Tyler Mark Pierson , Meena Balasubramanian AMERICAN JOURNAL OF MEDICAL GENETICS PART A(2023)
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