AlyceVictoriaBelonisMD

PubMed

• 2 citations
  Clinico-biological refinement of BCL11B-related disorder and identification of an episignature: A series of 20 unreported individuals.
  Quentin Sabbagh, Sadegheh Haghshenas, Juliette Piard, Chloé Trouvé, Jeanne Amiel, Tania Attié-Bitach, Tugce Balci, Mouna Barat-Houari, Alyce Belonis, Odile Boute, Dian...> ;Genetics in Medicine. 2024 Jan 1
• Genetics 101: When to Refer.
  Alyce Belonis, Sofia Saenz Ayala> ;Pediatric Clinics of North America. 2023 Oct 1
• 2 citations
  Exome sequencing identified a novel HIST1H1E heterozygous protein-truncating variant in a 6-month-old male patient with Rahman syndrome: A case report.
  Subba Rao Indugula, Sofia Saenz Ayala, Francesco Vetrini, Alyce Belonis, Wenying Zhang> ;Clinical Case Reports. 2022 Feb 1
• 1 citations
  Clinically available testing options resulting in diagnosis in post-exome clinic at one medical center.
  Elizabeth K Baker, Elizabeth A Ulm, Alyce Belonis, Diana S Brightman, Barbara E Hallinan, Nancy D Leslie, Alexander G Miethke, Marissa Vawter-Lee, Yaning Wu, Loren D M...> ;Frontiers in Genetics. 2022 Jan 1
• 3 citations
  Rotational Position of the Aortic Root is Associated with Increased Aortic Dimensions in Marfan and Loeys–Dietz Syndrome
  Shannon K Powell, Hassan Almeneisi, Tarek Alsaied, Amy R. Shikany, Laura Riley, Erin M. Miller, Alyce Belonis, Kathryn Nicole Weaver, Nicole Brown, Shumpei Mori, Justi...> ;Pediatric Cardiology. 2021 Apr 13
• 1 citations
  An unusual cause for Coffin-Lowry syndrome: Three brothers with a novel microduplication in RPS6KA3.
  Valerie J. Castelluccio, Francesco Vetrini, Ty C. Lynnes, Julie R. Jones, Lynda Holloway, Alyce Belonis, Amy M. Breman, Brett H. Graham, Katherine Sapp, Theodore E. Wi...> ;American Journal of Medical Genetics. Part A. 2019 Dec 1
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