Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Silver-Russell Syndrome and DLK1[original query] |
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Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients. Clinical epigenetics 2020 6 12 (1): 86. Inoue Takanobu, Nakamura Akie, Iwahashi-Odano Megumi, Tanase-Nakao Kanako, Matsubara Keiko, Nishioka Junko, Maruo Yoshihiro, Hasegawa Yukihiro, Suzumura Hiroshi, Sato Seiji, Kobayashi Yoshiyuki, Murakami Nobuyuki, Nakabayashi Kazuhiko, Yamazawa Kazuki, Fuke Tomoko, Narumi Satoshi, Oka Akira, Ogata Tsutomu, Fukami Maki, Kagami Masa |
Screening of patients born small for gestational age with the Silver-Russell syndrome phenotype for DLK1 variants. European journal of human genetics : EJHG 2021 7 29 (12): 1756-1761. Pham Aurélie, Sobrier Marie-Laure, Giabicani Eloïse, Le Jules Fernandes Marilyne, Mitanchez Delphine, Brioude Fréderic, Netchine Irè |
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- Page last updated:Apr 29, 2024
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