Standard
Missense mutations in the BCS1L gene as a cause of the Bjornstad syndrome. / Hinson, J.T.; Fantin, V.R.; Schonberger, J.; Breivik, N.; Siem, G.; McDonough, B.; Sharma, P.; Keogh, I.; Godinho, R.; Santos, F.; Esparza, A.; Nicolau, Y.; Selvaag, E.; Cohen, B.H.; Hoppel, C.L.; Tranebjærg, Lisbeth; Eavey, R.D.; Seidman, J.G.; Seidman, C.E.
I:
New England Journal of Medicine, Bind 356, Nr. 8, 2007, s. 809-819.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Harvard
Hinson, JT, Fantin, VR, Schonberger, J, Breivik, N, Siem, G, McDonough, B, Sharma, P, Keogh, I, Godinho, R, Santos, F, Esparza, A, Nicolau, Y, Selvaag, E, Cohen, BH, Hoppel, CL, Tranebjærg, L, Eavey, RD, Seidman, JG & Seidman, CE 2007, 'Missense mutations in the BCS1L gene as a cause of the Bjornstad syndrome', New England Journal of Medicine, bind 356, nr. 8, s. 809-819.
APA
Hinson, J. T., Fantin, V. R., Schonberger, J., Breivik, N., Siem, G., McDonough, B., Sharma, P., Keogh, I., Godinho, R., Santos, F., Esparza, A., Nicolau, Y., Selvaag, E., Cohen, B. H., Hoppel, C. L., Tranebjærg, L., Eavey, R. D., Seidman, J. G., & Seidman, C. E. (2007). Missense mutations in the BCS1L gene as a cause of the Bjornstad syndrome. New England Journal of Medicine, 356(8), 809-819.
Vancouver
Hinson JT, Fantin VR, Schonberger J, Breivik N, Siem G, McDonough B o.a. Missense mutations in the BCS1L gene as a cause of the Bjornstad syndrome. New England Journal of Medicine. 2007;356(8):809-819.
Author
Hinson, J.T. ; Fantin, V.R. ; Schonberger, J. ; Breivik, N. ; Siem, G. ; McDonough, B. ; Sharma, P. ; Keogh, I. ; Godinho, R. ; Santos, F. ; Esparza, A. ; Nicolau, Y. ; Selvaag, E. ; Cohen, B.H. ; Hoppel, C.L. ; Tranebjærg, Lisbeth ; Eavey, R.D. ; Seidman, J.G. ; Seidman, C.E. / Missense mutations in the BCS1L gene as a cause of the Bjornstad syndrome. I: New England Journal of Medicine. 2007 ; Bind 356, Nr. 8. s. 809-819.
Bibtex
@article{260eae9020ec11ddbc23000ea68e967b,
title = "Missense mutations in the BCS1L gene as a cause of the Bjornstad syndrome",
abstract = "Udgivelsesdato: 2007/2/22",
author = "J.T. Hinson and V.R. Fantin and J. Schonberger and N. Breivik and G. Siem and B. McDonough and P. Sharma and I. Keogh and R. Godinho and F. Santos and A. Esparza and Y. Nicolau and E. Selvaag and B.H. Cohen and C.L. Hoppel and Lisbeth Tranebj{\ae}rg and R.D. Eavey and J.G. Seidman and C.E. Seidman",
year = "2007",
language = "English",
volume = "356",
pages = "809--819",
journal = "New England Journal of Medicine",
issn = "0028-4793",
publisher = "Massachusetts Medical Society",
number = "8",
}
RIS
TY - JOUR
T1 - Missense mutations in the BCS1L gene as a cause of the Bjornstad syndrome
AU - Hinson, J.T.
AU - Fantin, V.R.
AU - Schonberger, J.
AU - Breivik, N.
AU - Siem, G.
AU - McDonough, B.
AU - Sharma, P.
AU - Keogh, I.
AU - Godinho, R.
AU - Santos, F.
AU - Esparza, A.
AU - Nicolau, Y.
AU - Selvaag, E.
AU - Cohen, B.H.
AU - Hoppel, C.L.
AU - Tranebjærg, Lisbeth
AU - Eavey, R.D.
AU - Seidman, J.G.
AU - Seidman, C.E.
PY - 2007
Y1 - 2007
N2 - Udgivelsesdato: 2007/2/22
AB - Udgivelsesdato: 2007/2/22
M3 - Journal article
VL - 356
SP - 809
EP - 819
JO - New England Journal of Medicine
JF - New England Journal of Medicine
SN - 0028-4793
IS - 8
ER -
