Sequence Analysis of Thyroid Transcription Factor-1 Gene Reveals Absence of Mutations in Patients with Thyroid Dysgenesis but Presence of Polymorphisms in the 5' Flanking Region and Intron
スポンサーリンク
概要
著者
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HISHINUMA Akira
Department of Clinical Laboratory Medicine, Dokkyo University School of Medicine
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IEIRI Tamio
Department of Clinical Laboratory Medicine, Dokkyo University School of Medicine
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KANNO Yumiko
Sumitomo Metal Bio-Science Inc.
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Ieiri Tamio
Department Of Clinical Laboratory Medicine Dokkyo University School Of Medicine
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KURIBAYASHI Takeo
Department of Pediatrics, Dokkyo University School of Medicine
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ONIGATA Kazumichi
Department of Pediatrics, Gunma University School of Medicine
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NAGASHIMA Kanji
Department of Pediatrics, Gunma University School of Medicine
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Nagashima K
Department Of Pediatrics Gunma University School Of Medicine
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Nagashima Kanji
Department Of Pediatrics Gunma University School Of Medicine
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Hishinuma Akira
獨協医科大学
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Hishinuma Akira
Department Of Clinical Laboratory Medicine Dokkyo Medical University
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Kuribayashi Takeo
Department Of Pediatrics Dokkyo University School Of Medicine
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Onigata K
Gunma Univ. School Of Medicine Maebashi Jpn
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Onigata Kazumichi
Department Of Pediatrics And Developmental Medicine Gunma University Graduate School Of Medicine
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Kuribayashi Takeo
獨協医科大学 小児科
関連論文
- A novel compound heterozygous mutation in the thyroglobulin gene resulting in congenital goitrous hypothyroidism with high serum triiodothyronine levels
- Sporadic Congenital Hyperthyroidism due to a Germline Mutation in the Thyrotropin Receptor Gene (Leu 512 Gln) in a Japanese Patient
- Missense Mutation (C1263R) in the Thyroglobulin Gene Causes Congenital Goiter with Mild Hypothyroidism by Impaired Intracellular Transport
- Sequence Analysis of Thyroid Transcription Factor-2 (TTF-2) Gene in Ten Patients with Congenital Hypothyroidism due to Thyroid Dysgenesis
- Sequence Analysis of Thyroid Transcription Factor-1 Gene Reveals Absence of Mutations in Patients with Thyroid Dysgenesis but Presence of Polymorphisms in the 5' Flanking Region and Intron
- A Novel Thyrotropin Receptor Germline Mutation (Asp617Tyr) Causing Hereditary Hyperthyroidism
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