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KCNK9 imprinting syndrome-further delineation of a possible treatable disorder.
Graham, John M; Zadeh, Neda; Kelley, Melissa; Tan, Ee Shien; Liew, Wendy; Tan, Victoria; Deardorff, Matthew A; Wilson, Golder N; Sagi-Dain, Lena; Shalev, Stavit A.
Affiliation
  • Graham JM; Department of Pediatrics, Harbor-UCLA Medical Center, Cedars-Sinai Medical Center, David Geffen School of Medicine at UCLA, Los Angeles, California. john.graham@cshs.org.
  • Zadeh N; Division of Medical Genetics, CHOC Children's Hospital, Orange, California.
  • Kelley M; KCNK9 Imprinting Syndrome Support Group, Irvine, California.
  • Tan ES; Department of Paediatric Medicine, KK Women's and Children's Hospital, Singapore.
  • Liew W; Department of Paediatric Medicine, KK Women's and Children's Hospital, Singapore.
  • Tan V; Department of Paediatric Medicine, KK Women's and Children's Hospital, Singapore.
  • Deardorff MA; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.
  • Wilson GN; Division of Clinical Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Sagi-Dain L; Department of Pediatrics, Texas Tech University Health Science Center, Lubbock, Texas.
  • Shalev SA; Medical City Hospital, Dallas, Texas.
Am J Med Genet A ; 170(10): 2632-7, 2016 10.
Article in En | MEDLINE | ID: mdl-27151206
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genomic Imprinting / Potassium Channels, Tandem Pore Domain / Genetic Diseases, Inborn Limits: Female / Humans / Infant / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2016 Type: Article
Fulltext
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XML
PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genomic Imprinting / Potassium Channels, Tandem Pore Domain / Genetic Diseases, Inborn Limits: Female / Humans / Infant / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2016 Type: Article