E-LIB Suche - Ergebnisse für: Trujillano, Daniel

1

Apophysitis Among Male Youth Soccer Players at an Elite Soc..:

Gudelis, Mindaugas ; Til Perez, Lluis ; Trujillano Cabello, Javier...
Reproducció del document publicat a: https://doi.org/10.1177/23259671211065063. , 2022

Link: http://hdl.handle.net/10..

2

The evolution of the ventilatory ratio is a prognostic fact..:

Torres Martí, Antoni ; Motos, Anna ; Riera, Jordi...
Reproducció del document publicat a: https://doi.org/10.1186/s13054-021-03727-x. , 2021

Link: http://hdl.handle.net/24..

3

Papel de Colgadura, Vol. 18:

Castillo Jiménez, Yancy ; Rincón Rincón, Carolina Rosa ; Rodríguez Castro, Sandra Viviana...
2011-9763. , 2019

Link: http://repository.icesi...

4

Sistema adaptativo de prevención de intrusos mediante Honey..:

Mayordomo Trujillano, Daniel
http://hdl.handle.net/10486/676764. , 2017

Link: http://hdl.handle.net/10..

5

Clinical exome sequencing: results from 2819 samples reflec..:

Trujillano, Daniel ; Bertoli-Avella, Aida M ; Kumar Kandaswamy, Krishna...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5255946/. , 2017

Link: http://www.ncbi.nlm.nih...

6

Homozygous Deletion of Exons 2 and 3 of NPC2 Associated wit..:

Hebbar, Malavika ; Prasada L, Harsha ; Bhowmik, Aneek Das...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6422680/. , 2016

Link: http://www.ncbi.nlm.nih...

7

Whole exome sequencing in a rare disease: A patient with an..:

Hekim, Nezih ; Batyraliev, Talantbek ; Trujillano, Daniel...
Omics-A Journal of Integrative Biology. , 2016

Link: https://hdl.handle.net/2..

8

Whole Exome Sequencing in a Rare Disease: A Patient with An..:

Hekim, Nezih ; Batyraliev, Talantbek ; Trujillano, Daniel...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4876547/. , 2016

Link: http://www.ncbi.nlm.nih...

9

A comprehensive global genotype–phenotype database for rare..:

Trujillano, Daniel ; Oprea, Gabriela‐Elena ; Schmitz, Yvonne...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5241210/. , 2016

Link: http://www.ncbi.nlm.nih...

10

Mutations in DCHS1 Cause Mitral Valve Prolapse:

Durst, Ronen ; Sauls, Kimberly ; Peal, David S...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4720389/. , 2015

Link: http://www.ncbi.nlm.nih...

11

Mutations in DCHS1 cause mitral valve prolapse:

Durst, Ronen ; Sauls, Kimberly ; Peal, David S...
info:eu-repo/semantics/altIdentifier/doi/10.1038/nature14670. , 2015

Link: https://hal.science/hal-..

12

Mendelian disease gene identification and diagnosis using t..:

Trujillano Lidón, Daniel, 1987-
http://hdl.handle.net/10803/295582. , 2015

Link: http://hdl.handle.net/10..

13

Mutations in DCHS1 cause mitral valve prolapse:

Durst, Ronen ; Sauls, Kimberly ; Peal, David S...
info:eu-repo/semantics/altIdentifier/doi/10.1038/nature14670. , 2015

Link: https://hal.science/hal-..

14

Mutations in DCHS1 cause mitral valve prolapse:

Durst, Ronen ; Sauls, Kimberly ; Peal, David S...
info:eu-repo/semantics/altIdentifier/doi/10.1038/nature14670. , 2015

Link: https://hal.archives-ouv..

15

Asparagine Synthetase Deficiency: New Inborn Errors of Meta..:

Alfadhel, Majid ; Alrifai, Muhammad Talal ; Trujillano, Daniel...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4486270/. , 2015

Link: http://www.ncbi.nlm.nih...