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Kagami-Ogata syndrome in a patient with 46,XX,t(2;14)(q11.2;q32.2)mat disrupting MEG3.
Omark, Jessica; Masunaga, Yohei; Hannibal, Mark; Shaw, Brandon; Fukami, Maki; Kato, Fumiko; Saitsu, Hirotomo; Kagami, Masayo; Ogata, Tsutomu.
Affiliation
  • Omark J; Division of Pediatric Genetics, Metabolism and Genomic Medicine, University of Michigan Medical School, Detroit, MI, USA.
  • Masunaga Y; Department of Pediatrics, Hamamatsu University School of Medicine, Hamamatsu, Japan.
  • Hannibal M; Division of Pediatric Genetics, Metabolism and Genomic Medicine, University of Michigan Medical School, Detroit, MI, USA.
  • Shaw B; Department of Pathology and Laboratory Medicine, Henry Ford Health System, Detroit, MI, USA.
  • Fukami M; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan.
  • Kato F; Department of Pediatrics, Hamamatsu University School of Medicine, Hamamatsu, Japan.
  • Saitsu H; Department of Biochemistry, Hamamatsu University School of Medicine, Hamamatsu, Japan.
  • Kagami M; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan.
  • Ogata T; Department of Pediatrics, Hamamatsu University School of Medicine, Hamamatsu, Japan. tomogata@hama-med.ac.jp.
J Hum Genet ; 66(4): 439-443, 2021 Apr.
Article in En | MEDLINE | ID: mdl-33067531
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Full text: 1 Database: MEDLINE Main subject: Translocation, Genetic / Chromosomes, Human, Pair 2 / Chromosomes, Human, Pair 14 / Chromosome Disorders / Uniparental Disomy / RNA, Long Noncoding Limits: Adolescent / Female / Humans / Newborn Language: En Journal: J Hum Genet Journal subject: GENETICA MEDICA Year: 2021 Type: Article Affiliation country: United States
Fulltext
Add to My VHL
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Full text: 1 Database: MEDLINE Main subject: Translocation, Genetic / Chromosomes, Human, Pair 2 / Chromosomes, Human, Pair 14 / Chromosome Disorders / Uniparental Disomy / RNA, Long Noncoding Limits: Adolescent / Female / Humans / Newborn Language: En Journal: J Hum Genet Journal subject: GENETICA MEDICA Year: 2021 Type: Article Affiliation country: United States