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in Am J Hum Genet

Rare variants in NR2F2 cause congenital heart defects in humans

  • S. Al Turki
  • A.K. Manickaraj
  • C.L. Mercer
  • S.S. Gerety
  • M.P. Hitz
  • S. Lindsay
  • L.C.A. D'Alessandro
  • G.J. Swaminathan
  • J. Bentham
  • A.K. Arndt
  • J. Low
  • J. Breckpot
  • M. Gewillig
  • B. Thienpont
  • H. Abdul-Khaliq
  • C. Harnack
  • K. Hoff
  • H.H. Kramer
  • S. Schubert
  • R. Siebert
  • O. Toka
  • C. Cosgrove
  • H. Watkins
  • A.M. Lucassen
  • I.M. O'Kelly
  • A.P. Salmon
  • F.A. Bu'Lock
  • J. Granados-Riveron
  • K. Setchfield
  • C. Thornborough
  • J.D. Brook
  • B. Mulder
  • S. Klaassen
  • S. Bhattacharya
  • K. Devriendt
  • D.F. Fitzpatrick
  • D.I. Wilson
  • S. Mital
  • M.E. Hurles
in PLoS ONE

Outlier-based identification of copy number variations using targeted resequencing in a small cohort of patients with tetralogy of fallot

  • V. Bansal
  • C. Dorn
  • M. Grunert
  • S. Klaassen
  • R. Hetzer
  • F. Berger
  • S.R. Sperling
in Am J Hum Genet

Reponse to De Leeuw and Houge

  • A.K. Arndt
  • C.A. Macrae
  • S. Klaassen