skip to main content
資源種類 顯示結果: 顯示結果: 查詢種類 索引
檢索結果 1 2 3 4 5 next page
精簡: 資源種類: 報告 刪除
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Material Type:
報告
加入個人書架

HIPAA Privacy Rule To Support Reproductive Health Care Privacy

The Federal Register / FIND, 2024, Vol.89 (82), p.32976

可取得全文

2
Material Type:
報告
加入個人書架

A bi-objective genetic approach for the selection of sugarcane varieties to comply with environmental and economic requirements

de Oliveira Florentino, H ; Pato, M V

Journal of the Operational Research Society: Special Issue: Sustainable Operations Management: Design Modelling and Analysis, 2014, Vol.65 (6), p.842-854

可取得全文

3
Material Type:
報告
加入個人書架

Clinical, histopathological, and genetic aspects in one case of ligneous conjunctivitis

Raimann, Rolf ; Moya, Rene ; Anguita, Rodrigo ; Kobus, Rudolf ; Pérez, Marcela ; Gonzalez, Patricio

Ophthalmic Genetics, 2018, Vol.39 (5), p.642-644

可取得全文

4
Material Type:
報告
加入個人書架

Principle-Based Ethics Framework for Access to and Use of Veteran Data

The Federal Register / FIND, 2022, Vol.87 (129), p.40451

可取得全文

5
Material Type:
報告
加入個人書架

A twofold update quantum-inspired genetic algorithm for efficient combinatorial optimal decisions in engineering system design and operations

Zou, Pan ; Jiao, Jianxin (Roger) ; Zhou, Feng

Journal of Engineering Design, 2023, Vol.34 (4), p.271-293

可取得全文

6
Material Type:
報告
加入個人書架

Genetic and cellular characterization of MscS-like putative channels in the filamentous fungus Aspergillus nidulans

Dionysopoulou, Mariangela ; Yan, Nana ; Wang, Bolin ; Pliotas, Christos ; Diallinas, George

Channels, 2022, Vol.16 (1), p.148-158

可取得全文

7
Material Type:
報告
加入個人書架

Combined Occurrence of Autosomal Dominant Aniridia and Autosomal Recessive Albinism in Several Members of a Family

Yahalom, Claudia ; Sharon, Dror ; Dalia, Eli ; Simhon, Shiran Ben ; Shemesh, Efrat ; Blumenfeld, Anat

Ophthalmic Genetics, 2015, Vol.36 (2), p.175-179

可取得全文

8
Material Type:
報告
加入個人書架

A novel MFRP gene variant in a family with posterior microphthalmos, retinitis pigmentosa, foveoschisis, and foveal hypoplasia

Godinho, Gonçalo ; Madeira, Carolina ; Grangeia, Ana ; Neves-Cardoso, Pedro ; Santos-Silva, Renato ; Brandão, Elisete ; Carneiro, Ângela ; Falcão-Reis, Fernando ; Estrela-Silva, Sérgio

Ophthalmic Genetics, 2020, Vol.41 (5), p.474-479

可取得全文

9
Material Type:
報告
加入個人書架

Genetic structure and forensic characteristics of the Korean population revealed by GoldenEye 20A

Xuan, Jin-Feng ; Adnan, Atif ; Zafar, Absar Ahmad ; He, Guanglin ; Li, Xiao-na

Annals of Human Biology, 2020, Vol.47 (6), p.560-563

可取得全文

10
Material Type:
報告
加入個人書架

Atypical Presentation of Sengers Syndrome: A Novel Mutation Revealed with Postmortem Genetic Testing

Guleray, Naz ; Kosukcu, Can ; Taskiran, Zihni Ekim ; Simsek Kiper, Pelin Ozlem ; Utine, Gulen Eda ; Gucer, Safak ; Tokatli, Aysegul ; Boduroglu, Koray ; Alikasifoglu, Mehmet

Fetal and Pediatric Pathology, 2020, Vol.39 (2), p.163-171

可取得全文

個人化查詢結果

  1. 個人化設定

Refine Search Results

擴展檢索範圍

  1.   

建立日期 

  1. 之前2002  (5)
  2. 2002到2006  (14)
  3. 2007到2011  (131)
  4. 2012到2017  (542)
  5. 之後 2017  (471)
  6. 更多選項 open sub menu

正在檢索遠程資料庫,請稍等

  • 查詢:
  • scope:("NUTN"),scope:(NUTN_ALEPH),scope:(NUTN_IR),scope:(NUTN_SFX),primo_central_multiple_fe
  • 顯示現有記錄