You are here

  • Home
  • Archive
  • Volume 56, Issue 2
  • Mapping of breakpoints in balanced chromosomal translocations by shallow whole-genome sequencing points to EFNA5, BAHD1 and PPP2R5E as novel candidates for genes causing human Mendelian disorders

Article metrics

Article menu

Download PDFPDF

Chromosomal rearrangements
Original article
Mapping of breakpoints in balanced chromosomal translocations by shallow whole-genome sequencing points to EFNA5, BAHD1 and PPP2R5E as novel candidates for genes causing human Mendelian disorders
Free

 

Online download statistics by month:

Online download statistics by month: October 2018 to March 2024

AbstractFullPdf
Oct 20185184532
Nov 20183564117
Dec 20183321813
Jan 201939520943
Feb 201922325358
Mar 201927430757
Apr 201912616332
May 201914618341
Jun 201912616234
Jul 201910713460
Aug 2019605726
Sep 2019575426
Oct 2019605621
Nov 2019605916
Dec 2019636026
Jan 2020605815
Feb 2020424218
Mar 2020615619
Apr 2020454111
May 2020757328
Jun 2020898732
Jul 2020524823
Aug 2020444415
Sep 2020555023
Oct 2020514711
Nov 2020413520
Dec 2020272410
Jan 2021302812
Feb 2021514526
Mar 2021333020
Apr 2021323216
May 2021483925
Jun 2021333217
Jul 2021373116
Aug 2021413327
Sep 2021343316
Oct 2021575433
Nov 2021423829
Dec 2021373111
Jan 2022503719
Feb 202229269
Mar 2022473414
Apr 2022343319
May 2022323113
Jun 2022454319
Jul 2022343110
Aug 2022494414
Sep 2022483913
Oct 2022464017
Nov 2022363314
Dec 202233248
Jan 2023312312
Feb 2023484513
Mar 2023413816
Apr 2023141417
May 202320177
Jun 2023111010
Jul 2023171411
Aug 2023322830
Sep 2023373219
Oct 202333269
Nov 202339259
Dec 2023423316
Jan 202444416
Feb 2024463310
Mar 2024272230
Total498536481359