Makita Yoshio 蒔田芳男

… Alternative Names

蒔田芳男マキタヨシオ

MAKITA Yoshio 蒔田芳男

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Researcher Number	20271778
Other IDs
External Links
Affiliation (Current)	2025: 旭川医科大学, 医学部, 教授
Affiliation (based on the past Project Information) *help	2024: 旭川医科大学, 医学部, 教授 2018 – 2021: 旭川医科大学, 医学部, 教授 2007 – 2010: Asahikawa Medical Collage, Education center, professor 2006: Asahikawa Medical College, Pediatrics, Research Associate, 医学部・小児科学講座, 助手 2005 – 2006: Asahikawa Medical College, School of Medicine, Pediatrics, Instructor, 医学部, 講師 2001 – 2004: 旭川医科大学, 医学部, 助手 1996 – 1998: 旭川医科大学, 医学部, 助手
Review Section/Research Field	Principal Investigator Pediatrics / Human genetics / Embryonic/Neonatal medicine Except Principal Investigator Basic Section 58010:Medical management and medical sociology-related / Pediatrics / Embryonic/Neonatal medicine / Biological Sciences / Human genetics / Pediatrics
Keywords	Principal Investigator SNP / isodisomy / 第6番染色体 / 新生児一過性糖尿病 / case control study / haplotype / multifactorial disease / Hirschsprung disease / SNPs / ケースコントロール解析 … More / 主効果遺伝子 / 関連解析 / ハプロタイプ / 多因子遺伝 / ケースコントロール研究 / パプロダイプ / 多因子疾患 / ヒルシュスプルング病 / 潜在性異常 / 奇形症候群 / アレイCGH法 / 染色体異常 / 先天異常 / paternal imprinting / paternal insprinting … More Except Principal Investigator SNP / ハプロタイプ / ゲノム / CGH / 遺伝的制御 / LH / 思春期発現 / haplotype / SNPs / HAMA / TSH / 子宮内発育不全 / 医療・福祉 / 遺伝疾患 / 均てん化 / 医療格差 / ICT / ゲノム医療 / 遠隔医療 / 教育評価 / シミュレーション教育 / ロールプレイ / ルーブリック / 模擬面接 / 遺伝カウンセリング / growth fator / intrauterine growth retardation / genome / medical / gene / 子宮内胎児発育遅延 / 遺伝的多い型 / type 1 insulin-like growth factor receptor / insulin-like growth factor II / insulin-like gorwth factor I / 胎児発育 / 成長因子 / 遺伝子 / BAC / Diagnostic tool / Microarray / Chromosome aberration / Autism / Mental retardation / Congenital anomaly / 網羅的解析 / 精神発達遅滞 / マイクロアレイ / 遺伝子診断 / 染色体異常 / steroidogenesis / Haplotype / genetic control / Pubertal onset / 性ステロイド産生 / FSH receptor / CG receptor / GnRH receptor / pubertal onset / 思春期発来 / FSH受容体 / CG受容体 / GnRH受容体 / haplotype association study / susceptible genes / essential hypertension / 連鎖不平衡 / ガイドライン / DOP-PCR / 本能性高血圧 / ゲノムワイド / 発症関連遺伝子 / LDブロック / 関連解析 / ハプロタイプ関連解析 / ハプロタイプ解析 / 感受性遺伝子 / 本態性高血圧 / false hyperthyrotropinemia / Anti-Mouse Antibody / Cretinism / Neonatal Mass-Screening / 抗TSH抗体 / 新生児マス・スクリーニング / 偽高TSH血症 / 抗マウス抗体 / クレチン症 / 新生児マススクリーニング / 11β-hdroxsteroid dehdroenase type2 / 11β-hydroxysteroid dehydrogenase type2 / 新生児 / 胎児 / グルコルチコイド / 副腎機能 / グルココルチコイド / 癌 / ゲノム一次構造異常 / Copy number variation / ゲノムコピー数異常 / Copy-number variation (CNV) / 潜在的コピー数異常 / BACアレイ / アレイCGH法 / 染色体 / 先天異常 / ゲノム構造異常 / アレイCGH / ヒトゲノム Less

Identification of issues and solution strategies for the development of genomic medicine in remote areas lacking in medical resources
- Principal Investigator
  
  山田崇弘
- Project Period (FY)
  2024 – 2026
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 58010:Medical management and medical sociology-related
- Research Institution
  Hokkaido University
Creation of genetic counseling role-play curriculum with rubric table
- Principal Investigator
  
  MIYAKE Hidehiko
- Project Period (FY)
  2018 – 2021
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 58010:Medical management and medical sociology-related
- Research Institution
  Ochanomizu University
New diagnostic approach for malformation syndromes and genome-wide search for syndrome specific genome imbalance using DNA microarrayPrincipal Investigator
- Principal Investigator
  
  MAKITA Yoshio
- Project Period (FY)
  2008 – 2010
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Embryonic/Neonatal medicine
- Research Institution
  Asahikawa Medical College
Impact of glucocorticoid exposure for fetus in fetal development and neonatal disease
- Principal Investigator
  
  NAGAYA Ken
- Project Period (FY)
  2008 – 2010
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Embryonic/Neonatal medicine
- Research Institution
  Asahikawa Medical College
Development and application of high-density genomic microarray system as a tool for human genome structural variation
- Principal Investigator
  
  IMOTO Issei
- Project Period (FY)
  2005 – 2009
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas
- Review Section
  
  Biological Sciences
- Research Institution
  Tokyo Medical and Dental University
Development of array based comparative genomic hybridization (CGH) as a diagnostic tool for cryptic chromosome aberrations in congenital disorders
- Principal Investigator
  
  INAZAWA Johji
- Project Period (FY)
  2005 – 2006
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Human genetics
- Research Institution
  Tokyo Medical and Dental University
The association between fetal and postnatal growth and polymorphisms of insulin-like growth factors
- Principal Investigator
  
  NAGAYA Ken, 竹田津原野
- Project Period (FY)
  2005 – 2007
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Embryonic/Neonatal medicine
- Research Institution
  Asahikawa Medical College
Analysis for molecular-pathogenesis of Hirschsprung disease. As a model of multifactorial diseasePrincipal Investigator
- Principal Investigator
  
  MAKITA Yoshio
- Project Period (FY)
  2003 – 2005
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Human genetics
- Research Institution
  Asahikawa Medical College
Relationship of genetic diversity of hypothalamo-pituitary-gonadal axis and puberatal onset
- Principal Investigator
  
  ITO Yoshiya
- Project Period (FY)
  2003 – 2004
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Asahikawa Medical College
Genetic control of pubertal onset : role of polymorphism of LH/CG and GnRH receptor gene
- Principal Investigator
  
  ITO Yoshiya
- Project Period (FY)
  2001 – 2002
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Asahikawa Medical College
Identification of susceptible genes for essential hypertension
- Principal Investigator
  
  HATA Akira
- Project Period (FY)
  2000 – 2004
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas
- Review Section
  
  Biological Sciences
- Research Institution
  Graduate School of Medicine, Chiba university
  Asahikawa Medical College
Pitfalls in Neonatal Mass-screening for Cretinism - False hyperthyrotropinemia caused by human anti-mouse antibody (HAMA) of meternal origin
- Principal Investigator
  
  ITO Yoshiya, 矢野公一
- Project Period (FY)
  1998 – 2000
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Asahikawa Medical College
新生児一過性糖尿病の表現型と第6番染色体isodisomyの関連Principal Investigator
- Principal Investigator
  
  蒔田芳男
- Project Period (FY)
  1997 – 1998
- Research Category
  
  Grant-in-Aid for Encouragement of Young Scientists (A)
- Research Field
  
  Pediatrics
- Research Institution
  Asahikawa Medical College
新生児一過性糖尿病の発症に第6番染色体のisodisomyが関与しているかPrincipal Investigator
- Principal Investigator
  
  蒔田芳男
- Project Period (FY)
  1996
- Research Category
  
  Grant-in-Aid for Encouragement of Young Scientists (A)
- Research Field
  
  Pediatrics
- Research Institution
  Asahikawa Medical College

All 2021 2019 2011 2010 2009 2008 2007 2005 2004

All Journal Article Presentation Book

[Book] 小児・新生児診療ゴールデンハンドブック(藤枝憲二、梶野浩樹編)(L染色体異常・奇形症候群、Part 2小児医療の実践)2009
- Author(s)
  蒔田芳男
- Publisher
  南江堂
- Data Source
  KAKENHI-PROJECT-20390301
[Book] ここまできた注目の小児科臨床ガイド小児科専門医のための生涯教育ナビゲータ(日本小児科学会教育委員会五十嵐隆編)(29.アレイCGH診断法の進歩 5章診断・検査医学の進歩)2009
- Author(s)
  蒔田芳男
- Publisher
  中山書店
- Data Source
  KAKENHI-PROJECT-20390301
[Book] アレイCGH診断活用ガイドブック-知って置きたい染色体微細構造異常症2008
- Author(s)
  稲澤譲治、蒔田芳男、羽田明編集
- Publisher
  医薬ジャーナル社
- Data Source
  KAKENHI-PROJECT-20390301
[Journal Article] 【成人学習理論から学ぶ臨床遺伝教育のこれから】到達目標　実践例として、教育目標の立て方　臨床遺伝専門医の新しい行動目標はどのようにしてつくられたのか?2021
- Author(s)
  三宅秀彦　蒔田芳男
- Journal Title
  
  遺伝子医学
  
  Volume: 11 Pages: 4549-4549
- Data Source
  KAKENHI-PROJECT-18K09997
[Journal Article] 5.78 Mb terminal deletion of chromosome 15q in a girl, evaluation of NR2F2 as candidate gene for congenital heart defects.2011
- Author(s)
  Nakamura E, Makita Y, 他
- Journal Title
  
  Eur J Med Genet.
  
  Volume: 54 Pages: 354-356
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390301
[Journal Article] Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies.2011
- Author(s)
  Hayashi S, Imoto I, Aizu Y, Okamoto N, Mizuno S, Kurosawa K, Honda S, Araki S, Mizutani S, Numabe H, Saitoh S, Kosho T, Fukushima Y, Mitsubuchi H, Endo F, Chinen Y, Kosaki R, Okuyama T, Ohki H, Yoshihashi H, Ono M, Takada F, Ono H, Yagi M, Matsumoto H, Makita Y, Hata A, Inazawa J.
- Journal Title
  
  J Hum Genet. 56(2)
  
  Pages: 110-24
- NAID
  10030657707
- Data Source
  KAKENHI-PROJECT-20390301
[Journal Article] 5.78 Mb terminal deletion of chromosome 15q in a girl, evaluation of NR2F2 as candidate gene for congenital heart defects.2011
- Author(s)
  Nakamura E, Makita Y, Okamoto T, Nagaya K, Hayashi T, Sugimoto M, Manabe H, Taketazu G, Kajino H, Fujieda K
- Journal Title
  
  Eur J Med Genet. 54(3)
  
  Pages: 354-6
- Data Source
  KAKENHI-PROJECT-20390301
[Journal Article] 原因不明多発奇形・精神遅滞症例を対象とした染色体微細構造異常解析における遺伝カウンセリング2009
- Author(s)
  金子実基子、鮫島希代子、西川智子、古谷憲孝、吉橋博史、蒔田芳男、羽田明、稲澤譲治、千代豪昭、黒澤健司
- Journal Title
  
  日本遺伝カウンセリング学会誌 29(2)
  
  Pages: 57-61
- Data Source
  KAKENHI-PROJECT-20390301
[Journal Article] The CASK gene harbored in a deletion detected by array-CGH as a potential candidate for a gene causative of X-linked dominant mental retardation.2008
- Author(s)
  Hayashi S, Mizuno S, Migita O, Okuyama T, Makita Y, Hata A, Imoto I, Inazawa J.
- Journal Title
  
  Am J Med Genet A. 146A(16)
  
  Pages: 2145-51
- Data Source
  KAKENHI-PROJECT-20390301
[Journal Article] Heterozygous deletion at 14q22. 1-q22. 3 including the BMP4 gene in a patient with psychomotor petardation, congenital corneal opacity and feet polysyndactyly.2008
- Author(s)
  Hayashi S, Okamoto N, Makita Y, Hata A, Imoto I, Inazawa J.
- Journal Title
  
  Am J Med Genet A 146A
  
  Pages: 2905-10
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17019014
[Journal Article] The CASK gene harbored in a deletion detected by array-CGH as a potential candidate for a gene causative of X-linked dominant mental retardation.2008
- Author(s)
  Hayashi S, Mizuno S, Migita O, Okuyama T, Makita Y, Hata A, Imoto I, Inazawa J.
- Journal Title
  
  Am J Med Genet A 146A
  
  Pages: 2145-51
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17019014
[Journal Article] Heterozygous deletion at 14q22.1-q22.3 including the BMP4 gene in a patient with psychomotor retardation, congenital corneal opacity and feet polysyndactyly.2008
- Author(s)
  Hayashi S, Okamoto N, Makita Y, Hata A, Imoto I, Inazawa J.
- Journal Title
  
  Am J Med Genet A. 146A(22)
  
  Pages: 2905-10
- Data Source
  KAKENHI-PROJECT-20390301
[Journal Article] Construction of a high-density and high-resolution human chromosome X array for comparative genomic hybridization analysis.2007
- Author(s)
  Hayashi S, Honda S, Minaguchi M, Makita Y, Okamoto N, Kosaki R, Okuyama T, Imoto I, Mizutani S, Inazawa J.
- Journal Title
  
  J Hum Genet 52
  
  Pages: 397-405
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17019014
[Journal Article] Fortuitous Detection of a Submicroscopic Deletion at 1q25 in a girl with Cornelia-de Lange syndrome carrying t(5;13)(p13. 1;q12. 1) by array-based comparative genomic hybridization.2007
- Author(s)
  Hayashi S, Ono M, Makita Y, Imoto I, Mizutani S, Inazawa J.
- Journal Title
  
  Am J Med Genet 143A
  
  Pages: 1191-7
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17019014
[Journal Article] 新生児スクリーニング検査2005
- Author(s)
  蒔田芳男
- Journal Title
  
  「日本臨床」増刊「遺伝子診療学」-遺伝子診断の進歩と遺伝子治療の展望増刊
  
  Pages: 104-108
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15590289
[Journal Article] Neonatal screening2005
- Author(s)
  Makita Y.
- Journal Title
  
  Nippon Rinsho. 63 Suppl12
  
  Pages: 104-8
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15590289
[Journal Article] 生命保険加入における遺伝情報の取り扱いに関する現状と問題点2004
- Author(s)
  蒔田芳男, 羽田明
- Journal Title
  
  日本マススクリーニング学会誌 14
  
  Pages: 17-23
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15590289
[Journal Article] Genetic discrimination in life insurance in Japan2004
- Author(s)
  Makita Y, Hata A
- Journal Title
  
  Journal of Japanese Society for Mass-screening 14(1)
  
  Pages: 17-23
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15590289
[Presentation] 標準化を目指した遺伝カウンセリングロールプレイ事例の解析2019
- Author(s)
  三宅秀彦四元淳子浦野真理櫻井晃洋蒔田芳男
- Organizer
  第５１回日本医学教育学会大会
- Data Source
  KAKENHI-PROJECT-18K09997
[Presentation] Xp11.2微細重複症候群の一例2010
- Author(s)
  岡本伸彦、林深、稲澤譲二、蒔田芳男、羽田明
- Organizer
  第55回日本人類遺伝学会
- Place of Presentation
  埼玉
- Data Source
  KAKENHI-PROJECT-20390301
[Presentation] 新規症候群の可能性がある10p12.1-p11.23欠失の2症例2010
- Author(s)
  岡本奈那、林深、本田尚三、小栗泉、長谷川知子、小崎里華、井本逸勢、蒔田芳男、羽田明、森山啓司、稲澤譲二
- Organizer
  第55回日本人類遺伝学会
- Place of Presentation
  埼玉
- Data Source
  KAKENHI-PROJECT-20390301
[Presentation] 複数のゲノムアレイによる先天異常疾患におけるゲノム構造異常2010
- Author(s)
  林深、岡本奈那、本田尚三、井本逸勢、蒔田芳男、羽田明、稲澤譲二
- Organizer
  第55回日本人類遺伝学会
- Place of Presentation
  埼玉
- Data Source
  KAKENHI-PROJECT-20390301
[Presentation] アレイCGH診断法実用化コンソーシアム先天奇形症候群診断用アレイ(GD700)の開発2010
- Author(s)
  蒔田芳男
- Organizer
  第114回日本小児科学会学術集会
- Place of Presentation
  盛岡
- Data Source
  KAKENHI-PROJECT-20390301
[Presentation] 新しい染色体微細欠失・重複症候群の発見と臨床応用2010
- Author(s)
  蒔田芳男
- Organizer
  分野別シンポジウム「先天性疾患における最近の進歩:病因解明から遺伝子診断へ」第114回日本小児科学会学術集会
- Place of Presentation
  盛岡
- Data Source
  KAKENHI-PROJECT-20390301
[Presentation] アレイCGHで診断された1p34.3微細欠失2009
- Author(s)
  岡本伸彦、林深、井本逸勢、稲澤譲治、蒔田芳男、羽田明
- Organizer
  第54回日本人類遺伝学会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-20390301
[Presentation] サブテロメア欠失症候群:1p36欠失症候群の1例2009
- Author(s)
  宮本晶恵、蒔田芳男、福田郁江、田中肇、岡隆治、長和彦、林深、井本逸勢、稲澤譲治
- Organizer
  第51回日本小児神経学会総会
- Place of Presentation
  米子
- Data Source
  KAKENHI-PROJECT-20390301
[Presentation] 小頭症と小脳脳幹部低形成を伴う発達遅滞12例におけるCASK遺伝子の解析2009
- Author(s)
  林深、岡本伸彦、水野誠司、小野正恵、小崎里華、奥山虎之、知念安紹、蒔田芳男、羽田明、井本逸勢、稲澤譲治
- Organizer
  第54回日本人類遺伝学会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-20390301
[Presentation] アレイCGH診断法実用化コンソーシアム GDA700による染色体微細異常解析受託システムの構築2009
- Author(s)
  会津善紀、井本逸勢、林深、小澤伸晃、左合治彦、山口敏和、永田欽也、宮本力、蒔田芳男、羽田明、稲澤譲治
- Organizer
  第54回日本人類遺伝学会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-20390301
[Presentation] 小頭症と小脳脳幹部低形成を呈するCASK異常症の臨床像2009
- Author(s)
  岡本伸彦、平井聡里、青天目信、荒井洋、林深、井本逸勢、稲澤譲治、蒔田芳男
- Organizer
  第51回日本小児神経学会総会
- Place of Presentation
  米子
- Data Source
  KAKENHI-PROJECT-20390301
[Presentation] 小頭症と小脳脳幹部低形成を伴う発達遅滞の原因遺伝子の候補であるCASKの解析2009
- Author(s)
  林深、岡本伸彦、水野誠司、小野正恵、小崎里華、奥山虎之、知念安紹、蒔田芳男、羽田明、井本逸勢、稲澤譲治
- Organizer
  第51回日本小児神経学会総会
- Place of Presentation
  米子
- Data Source
  KAKENHI-PROJECT-20390301
[Presentation] ゲノムアレイを用いた精神遅滞の診断プラットフォームの開発2009
- Author(s)
  蒔田芳男、斉藤伸治、羽田明、吉橋博史、黒澤健司、小崎里華、小野正恵、沼部博直、水野誠司、福嶋義光、岡本伸彦、三渕浩、知念安紹、林深、井本逸勢、稲澤譲治
- Organizer
  第112回日本小児科学会学術集会
- Place of Presentation
  奈良
- Data Source
  KAKENHI-PROJECT-20390301
[Presentation] アレイCGH法を用いた多発奇形を伴う精神遅滞症例解析の4年間の実績2009
- Author(s)
  林深、岡本奈那、本田尚三、蒔田芳男、羽田明、井本逸勢、稲澤譲治
- Organizer
  第54回日本人類遺伝学会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-20390301
[Presentation] 新規症候群の可能性のある10q24微細欠失を伴う2症例の報告2009
- Author(s)
  岡本奈那、林深、黒澤健司、水野誠司、蒔田芳男、羽田明、井本逸勢、森山啓司、稲澤譲治
- Organizer
  第54回日本人類遺伝学会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-20390301
[Presentation] アレイCGHを用いた多発奇形を伴う精神遅滞症例解析5年間の実績2009
- Author(s)
  林深、本田尚三、井本逸勢、蒔田芳男、羽田明、稲澤譲治
- Organizer
  第112回日本小児科学会学術集会
- Place of Presentation
  奈良
- Data Source
  KAKENHI-PROJECT-20390301
[Presentation] 新しい染色体微細欠失・重複症候群の発見と臨床応用2008
- Author(s)
  蒔田芳男, 他
- Organizer
  第53回日本人類遺伝学会シンポジウムXI進化する細胞遺伝学
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-20390301
[Presentation] 新しい染色体微細欠失・重複症候群の発見と臨床応用2008
- Author(s)
  蒔田芳男
- Organizer
  シンポジウムXI 進化する細胞遺伝学第53回日本人類遺伝学会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-20390301
[Presentation] ゲノムアレイを用いた先天異常症の効率的診断法の確立と疾患特異的構造異常の探索2008
- Author(s)
  蒔田芳男、斉藤伸治、羽田明、石井拓麿、吉橋博史、黒澤健司、小崎里華、小野正恵、沼部博直、水野誠司、古庄知己、福嶋義光、岡本伸彦、三渕浩、知念安紹、林深、井本逸勢、稲澤譲治
- Organizer
  第53回日本人類遺伝学会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-20390301
[Presentation] 商用プローブにてモザイクが検出されたMiller-Dieker症候群の1例2008
- Author(s)
  蒔田芳男、長屋建、高橋悟、藤枝憲二、林深、井本逸勢、稲澤譲治
- Organizer
  第53回日本人類遺伝学会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-20390301
[Presentation] ゲノムアレイを用いた先天異常症の効率的診断法の確立と疾患特異的構造異常の探索2008
- Author(s)
  蒔田芳男、藤枝憲二、斉藤伸治、羽田明、石井拓麿、吉橋博史、黒澤健司、小崎里華、小野正恵、沼部博直、水野誠司、古庄知己、福嶋義光、岡本伸彦、三渕浩、知念安紹、林深、井本逸勢、稲澤譲治
- Organizer
  第111回日本小児科学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-20390301

1. ITO Yoshiya (70241437)

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Makita Yoshio 蒔田 芳男

蒔田 芳男 マキタ ヨシオ

MAKITA Yoshio 蒔田 芳男

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New diagnostic approach for malformation syndromes and genome-wide search for syndrome specific genome imbalance using DNA microarrayPrincipal Investigator

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Analysis for molecular-pathogenesis of Hirschsprung disease. As a model of multifactorial diseasePrincipal Investigator

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新生児一過性糖尿病の表現型と第6番染色体isodisomyの関連Principal Investigator

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新生児一過性糖尿病の発症に第6番染色体のisodisomyが関与しているかPrincipal Investigator

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Makita Yoshio 蒔田芳男

蒔田芳男マキタヨシオ

MAKITA Yoshio 蒔田芳男

[Book] 小児・新生児診療ゴールデンハンドブック(藤枝憲二、梶野浩樹編)(L染色体異常・奇形症候群、Part 2小児医療の実践)2009

[Book] ここまできた注目の小児科臨床ガイド小児科専門医のための生涯教育ナビゲータ(日本小児科学会教育委員会五十嵐隆編)(29.アレイCGH診断法の進歩 5章診断・検査医学の進歩)2009

[Journal Article] 【成人学習理論から学ぶ臨床遺伝教育のこれから】到達目標　実践例として、教育目標の立て方　臨床遺伝専門医の新しい行動目標はどのようにしてつくられたのか?2021