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Tags: 2015, Ackerman K G, Andrews D, clinical genetics, Coletti C M, congenital diaphragmatic hernia, Darvishi K, defects, DNA copy number variation, Donahoe P K, Exome, fallot, FOG2, gene, Genetics & Heredity, High F A, Kashani A, Lage K, Lee C, Longoni M, Loscertales M, Maalouf F I, penetrance, Pober B R, Russell M K, tetralogy, Tracy A A, variants, Ward-Melver C, Woods S A, ZFPM2
Tags: 2019, Akron Children's Hospital, Bertini Enrico Silvio, Chinnery Patrick F, Christodoulou John, clinical genetics, Cohen Bruce H, Davis Ryan L, Department of Integrative Medical Sciences, Department of Pediatrics, Diagnosis, evidence based practice, Falk Marni J, Fratter Carl, Goldstein Amy, Horvath Rita, Journal of medical genetics, Karaa Amel, Koenig Mary Kay, Mancuso Michaelangelo, McCormack Shana, McCormick Elizabeth M, McFarland Robert, metabolic disorders, NEOMED College of Medicine, Nesbitt Victoria, Parikh Sumit, Rahman Shamima, Schiff Manuel, Steele Hannah, Stockler Silvia, Sue Carolyn, Tarnopolsky Mark, Thorburn David R, Vockley Jerry
Tags: 2019, Akron Children's Hospital, Bertini Enrico Silvio, Chinnery Patrick F, Christodoulou John, clinical genetics, Cohen Bruce H, Davis Ryan L, Department of Integrative Medical Sciences, Department of Pediatrics, Diagnosis, evidence based practice, Falk Marni J, Fratter Carl, Goldstein Amy, Horvath Rita, Journal of medical genetics, Karaa Amel, Koenig Mary Kay, Mancuso Michaelangelo, McCormack Shana, McCormick Elizabeth M, McFarland Robert, metabolic disorders, NEOMED College of Medicine, Nesbitt Victoria, Parikh Sumit, Rahman Shamima, Schiff Manuel, Steele Hannah, Stockler Silvia, Sue Carolyn, Tarnopolsky Mark, Thorburn David R, Vockley Jerry