1. 4D Trajectory Design for Vision Only Sense and Avoid Flight Test *. Issue 1 (July 2017) Authors: Melczer, Mark; Bauer, Peter; Bokor, Jozsef Journal: IFAC-PapersOnLine Issue: Volume 50:Issue 1(2017) Page Start: 15203 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A Baseline for Global Weather and Climate Simulations at 1 km Resolution. (30th October 2020) Authors: Wedi, Nils P.; Polichtchouk, Inna; Dueben, Peter; Anantharaj, Valentine G.; Bauer, Peter; Boussetta, Souhail; Browne, Philip; Deconinck, Willem; Gaudin, Wayne; Hadade, Ioan; Hatfield, Sam; Iffrig, Olivier; Lopez, Philippe; Maciel, Pedro; Mueller, Andreas; Saarinen, Sami; Sandu, Irina; Quintino, T... Journal: Journal of advances in modeling earth systems Issue: Volume 12:Number 11(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A comparison of the regional Arctic System Reanalysis and the global ERA‐Interim Reanalysis for the Arctic1. (26th March 2015) Authors: Bromwich, David H.; Wilson, Aaron B.; Bai, Le‐Sheng; Moore, George W. K.; Bauer, Peter Journal: Quarterly journal of the Royal Meteorological Society Issue: Volume 142:Number 695(2016) Page Start: 644 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A disorder clinically resembling cystic fibrosis caused by biallelic variants in the AGR2 gene. Issue 10 (24th December 2021) Authors: Bertoli-Avella, Aida; Hotakainen, Ronja; Al Shehhi, Maryam; Urzi, Alice; Pareira, Catarina; Marais, Anett; Al Shidhani, Khoula; Aloraimi, Sumaya; Morales-Torres, Galina; Fisher, Steffen; Demuth, Laura; Moteleb Selim, Laila Abdel; Al Menabawy, Nihal; Busehail, Maryam; AlShaikh, Mohammed; Gilani, N... Journal: Journal of medical genetics Issue: Volume 59:Issue 10(2022) Page Start: 993 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. A hexanucleotide repeat modifies expressivity of X‐linked dystonia parkinsonism. Issue 6 (3rd May 2019) Authors: Westenberger, Ana; Reyes, Charles Jourdan; Saranza, Gerard; Dobricic, Valerija; Hanssen, Henrike; Domingo, Aloysius; Laabs, Björn‐Hergen; Schaake, Susen; Pozojevic, Jelena; Rakovic, Aleksandar; Grütz, Karen; Begemann, Kimberly; Walter, Uwe; Dressler, Dirk; Bauer, Peter; Rolfs, Arndt; Münchau, Ale... Journal: Annals of neurology Issue: Volume 85:Issue 6(2019) Page Start: 812 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. A homozygous frameshift variant in an alternatively spliced exon of DLG5 causes hydrocephalus and renal dysplasia. Issue 5 (21st February 2019) Authors: Yüksel, Zafer; Vogel, Florian; Alhashem, Amal M.; Alanzi, Talal S.A.; Tabarki, Brahim; Kampe, Kapil; Kandaswamy, Krishna K.; Werber, Martin; Bertoli‐Avella, Aida M.; Beetz, Christian; Rolfs, Arndt; Bauer, Peter Journal: Clinical genetics Issue: Volume 95:Issue 5(2019) Page Start: 631 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. ADAMTS19‐associated heart valve defects: Novel genetic variants consolidating a recognizable cardiac phenotype. Issue 1 (19th May 2020) Authors: Massadeh, Salam; Alhashem, Amal; van de Laar, Ingrid M.B.H.; Alhabshan, Fahad; Ordonez, Natalia; Alawbathani, Salem; Khan, Suliman; Kabbani, Mohamed S.; Chaikhouni, Farah; Sheereen, Atia; Almohammed, Iman; Alghamdi, Bader; Frohn‐Mulder, Ingrid; Ahmad, Salim; Beetz, Christian; Bauer, Peter; Wessel... Journal: Clinical genetics Issue: Volume 98:Issue 1(2020) Page Start: 56 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Adaptive paediatric investigation plans, a small step to improve regulatory decision making in drug development for children?. (12th July 2016) Authors: Bauer, Peter; König, Franz Journal: Pharmaceutical statistics Issue: Volume 15:Number 5(2016) Page Start: 384 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. An X‐linked syndrome with severe neurodevelopmental delay, hydrocephalus, and early lethality caused by a missense variation in the OTUD5 gene. Issue 2 (9th November 2020) Authors: Tripolszki, Kornelia; Sasaki, Erina; Hotakainen, Ronja; Kassim, Abdul Halim; Pereira, Catarina; Rolfs, Arndt; Bauer, Peter; Reardon, William; Bertoli‐Avella, Aida M. Journal: Clinical genetics Issue: Volume 99:Issue 2(2021) Page Start: 303 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Analysis of Polymorphisms in the Lactotransferrin Gene Promoter and Dental Caries. (8th December 2011) Authors: Brancher, João Armando; Pecharki, Giovana Daniela; Doetzer, Andrea Duarte; Medeiros, Kamilla Gabriella dos Santos; Cordeiro Júnior, Carlos Alberto; Sotomaior, Vanessa Santos; Bauer, Peter; Trevilatto, Paula Cristina Other Names: Vieira Alexandre Rezende Academic Editor. Journal: International journal of dentistry Issue: Volume 2011(2011) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗