Dergi makalesi Açık Erişim

De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development

Gordon, Christopher T.; Xue, Shifeng; Yigit, Goekhan; Filali, Hicham; Chen, Kelan; Rosins, Nadine; Yoshiura, Koh-ichiro; Oufadem, Myriam; Beck, Tamara J.; McGowan, Ruth; Magee, Alex C.; Altmueller, Janine; Dion, Camille; Thiele, Holger; Gurzau, Alexandra D.; Nuernberg, Peter; Meschede, Dieter; Muehlbauer, Wolfgang; Okamoto, Nobuhiko; Varghese, Vinod; Varghese, Vinod


BibTeX

@article{gordon_christopher_t_2017_46185,
  author       = {Gordon, Christopher T. and
                  Xue, Shifeng and
                  Yigit, Goekhan and
                  Filali, Hicham and
                  Chen, Kelan and
                  Rosins, Nadine and
                  Yoshiura, Koh-ichiro and
                  Oufadem, Myriam and
                  Beck, Tamara J. and
                  McGowan, Ruth and
                  Magee, Alex C. and
                  Altmueller, Janine and
                  Dion, Camille and
                  Thiele, Holger and
                  Gurzau, Alexandra D. and
                  Nuernberg, Peter and
                  Meschede, Dieter and
                  Muehlbauer, Wolfgang and
                  Okamoto, Nobuhiko and
                  Varghese, Vinod and
                  Varghese, Vinod},
  title        = {{De novo mutations in SMCHD1 cause Bosma arhinia 
                   microphthalmia syndrome and abrogate nasal
                   development}},
  journal      = {NATURE GENETICS},
  year         = 2017,
  volume       = 49,
  number       = 2,
  pages        = {249-255},
  month        = jan,
}
14
8
görüntülenme
indirilme
Görüntülenme 14
İndirme 8
Veri hacmi 3.2 kB
Tekil görüntülenme 13
Tekil indirme 8

Alıntı yap