Novel insights into the phenotypic spectrum and pathogenesis of Hardikar syndrome.

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Bibliographic Details
Title: Novel insights into the phenotypic spectrum and pathogenesis of Hardikar syndrome.
Authors: Strong A; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA. Electronic address: strong.alanna@gmail.com., March ME; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA., Cardinale CJ; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA., Liu Y; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA., Battig MR; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA., Finoti LS; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA., Matsuoka LS; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA., Watson D; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA., Sridhar S; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA., Jarrett JF; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA., Cannon I; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA., Li D; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA., Bhoj E; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA., Zackai EH; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA., Rand EB; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA; Division of Gastroenterology and Hepatology, Children's Hospital of Philadelphia, Philadelphia, PA., Wenger T; Division of Genetic Medicine, University of Washington, Seattle, WA., Lerman BB; Department of Medicine, Division of Cardiology, Greenberg Institute for Cardiac Electrophysiology, Cornell University Medical Center, New York, NY., Shikany A; Division of Cardiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH., Weaver KN; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH., Hakonarson H; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA; Division of Pulmonary Medicine, Children's Hospital of Philadelphia, Philadelphia, PA. Electronic address: hakonarson@chop.edu.
Source: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2024 Oct; Vol. 26 (10), pp. 101222. Date of Electronic Publication: 2024 Jul 20.
Publication Type: Journal Article
Journal Info: Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1530-0366
DOI:10.1016/j.gim.2024.101222