E-LIB Suche - Ergebnisse für: Juan, W-H.

1

Livedoid vasculopathy: long-term follow-up results followin..:

Juan, W-H. ; Chan, Y-S. ; Lee, J.C....
British Journal of Dermatology. 154 (2005) 2 - p. 251-255 , 2005

Link: https://doi.org/10.1111/..

2

Mapping and analysis of Caenorhabditis elegans transcriptio..:

Narasimhan, Kamesh ; Lambert, Samuel A ; Yang, Ally WH...
eLife. 4 (2015) - p. , 2015

Link: https://doi.org/10.7554/..

3

Subcortical volumes across the lifespan: Data from 18,605 h..:

Dima, D ; Modabbernia, A ; Papachristou, E...
https://discovery.ucl.ac.uk/id/eprint/10121892/1/hbm.25320.pdf. , 2022

Link: https://discovery.ucl.ac..

4

Cortical thickness across the lifespan: Data from 17,075 he..:

Frangou, S ; Modabbernia, A ; Williams, SCR...
https://discovery.ucl.ac.uk/id/eprint/10123032/1/hbm.25364.pdf. , 2022

Link: https://discovery.ucl.ac..

5

Subcortical volumes across the lifespan: Data from 18,605 h..:

Dima, D ; Modabbernia, A ; Papachristou, E...
issn:1065-9471. , 2021

Link: http://hdl.handle.net/11..

6

Cortical thickness across the lifespan: Data from 17,075 he..:

Frangou, S ; Modabbernia, A ; Williams, SCR...
issn:1065-9471. , 2021

Link: http://hdl.handle.net/11..

7

Whole-genome sequencing of a sporadic primary immunodeficie..:

Thaventhiran, JED ; Lango Allen, H ; Burren, OS...
https://discovery.ucl.ac.uk/id/eprint/10100106/1/PID_Nature_accepted_merged.pdf. , 2020

Link: https://discovery.ucl.ac..

8

Whole-genome sequencing of patients with rare diseases in a..:

Turro, E ; Astle, WJ ; Megy, K...
https://discovery.ucl.ac.uk/id/eprint/10103489/1/Gale_Whole-genome%20sequencing%20of%20patients%20with%20rare%20diseases%20in%20a%20national%20health%20system_AAM.pdf. , 2020

Link: https://discovery.ucl.ac..

9

Whole genome sequencing reveals that genetic conditions are..:

French, CE ; Delon, I ; Dolling, H...
doi:10.1007/s00134-019-05552-x. , 2019

Link: https://doi.org/10.1007/..

10

Complex structural variants in Mendelian disorders: identif..:

Sanchis-Juan, A ; Stephens, J ; French, CE...
https://discovery.ucl.ac.uk/id/eprint/10071523/7/Arno_Complex%20structural%20variants%20in%20Mendelian%20disorders.%20Identification%20and%20breakpoint%20resolution%20using%20short-%20and%20long-read%20genome%20sequencing_VoR.pdf. , 2018

Link: https://discovery.ucl.ac..

11

De novo truncating mutations in WASF1 cause intellectual di..:

Ito, Y ; Carss, KJ ; Duarte, ST...
doi:10.1016/j.ajhg.2018.06.001. , 2018

Link: https://doi.org/10.1016/..

12

De Novo Truncating Mutations in WASF1 Cause Intellectual Di..:

Ito, Y ; Carss, KJ ; Duarte, ST...
https://discovery.ucl.ac.uk/id/eprint/10051436/1/Gale%20VoR%201-s2.0-S0002929718301940-main.pdf. , 2018

Link: https://discovery.ucl.ac..

13

Comprehensive Rare Variant Analysis via Whole-Genome Sequen..:

Carss, KJ ; Arno, G ; Erwood, M...
https://discovery.ucl.ac.uk/id/eprint/1535962/1/Carss_Comprehensive_Rare_Variant_Analysis.pdf. , 2017

Link: https://discovery.ucl.ac..

14

Comprehensive Rare Variant Analysis via Whole-Genome Sequen..:

Carss, KJ ; Arno, G ; Erwood, M...
https://www.repository.cam.ac.uk/handle/1810/262688. , 2017

Link: https://www.repository.c..

15

Comprehensive Rare Variant Analysis via Whole-Genome Sequen..:

Carss, KJ ; Arno, G ; Erwood, M...
https://eprints.whiterose.ac.uk/136202/1/Carss_Comprehensive_Rare_Variant_Analysis.pdf. , 2017

Link: https://eprints.whiteros..