Standard
Breakpoint cloning and haplotype analysis indicate a single origin of the common Inv(10)( p11.2q21.2) mutation among northern Europeans. / Gilling, Mette; Dullinger, J.S.; Gesk, S.; Metzke-Heidemann, S.; Siebert, R.; Meyer, T.; Brondum-Nielsen, K.; Tommerup, Niels; Ropers, H.H.; Tümer, Zeynep; Kalscheuer, V.M.; Thomas, N.S.
I:
American Journal of Human Genetics, Bind 78, Nr. 5, 2006, s. 878-883.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Harvard
Gilling, M, Dullinger, JS, Gesk, S, Metzke-Heidemann, S, Siebert, R, Meyer, T, Brondum-Nielsen, K, Tommerup, N, Ropers, HH, Tümer, Z, Kalscheuer, VM & Thomas, NS 2006, 'Breakpoint cloning and haplotype analysis indicate a single origin of the common Inv(10)( p11.2q21.2) mutation among northern Europeans', American Journal of Human Genetics, bind 78, nr. 5, s. 878-883.
APA
Gilling, M., Dullinger, J. S., Gesk, S., Metzke-Heidemann, S., Siebert, R., Meyer, T., Brondum-Nielsen, K., Tommerup, N., Ropers, H. H., Tümer, Z., Kalscheuer, V. M., & Thomas, N. S. (2006). Breakpoint cloning and haplotype analysis indicate a single origin of the common Inv(10)( p11.2q21.2) mutation among northern Europeans. American Journal of Human Genetics, 78(5), 878-883.
Vancouver
Gilling M, Dullinger JS, Gesk S, Metzke-Heidemann S, Siebert R, Meyer T o.a. Breakpoint cloning and haplotype analysis indicate a single origin of the common Inv(10)( p11.2q21.2) mutation among northern Europeans. American Journal of Human Genetics. 2006;78(5):878-883.
Author
Gilling, Mette ; Dullinger, J.S. ; Gesk, S. ; Metzke-Heidemann, S. ; Siebert, R. ; Meyer, T. ; Brondum-Nielsen, K. ; Tommerup, Niels ; Ropers, H.H. ; Tümer, Zeynep ; Kalscheuer, V.M. ; Thomas, N.S. / Breakpoint cloning and haplotype analysis indicate a single origin of the common Inv(10)( p11.2q21.2) mutation among northern Europeans. I: American Journal of Human Genetics. 2006 ; Bind 78, Nr. 5. s. 878-883.
Bibtex
@article{de0cf99070eb11dcbee902004c4f4f50,
title = "Breakpoint cloning and haplotype analysis indicate a single origin of the common Inv(10)( p11.2q21.2) mutation among northern Europeans",
abstract = "Udgivelsesdato: 2006/5",
author = "Mette Gilling and J.S. Dullinger and S. Gesk and S. Metzke-Heidemann and R. Siebert and T. Meyer and K. Brondum-Nielsen and Niels Tommerup and H.H. Ropers and Zeynep T{\"u}mer and V.M. Kalscheuer and N.S. Thomas",
year = "2006",
language = "English",
volume = "78",
pages = "878--883",
journal = "American Journal of Human Genetics",
issn = "0002-9297",
publisher = "Cell Press",
number = "5",
}
RIS
TY - JOUR
T1 - Breakpoint cloning and haplotype analysis indicate a single origin of the common Inv(10)( p11.2q21.2) mutation among northern Europeans
AU - Gilling, Mette
AU - Dullinger, J.S.
AU - Gesk, S.
AU - Metzke-Heidemann, S.
AU - Siebert, R.
AU - Meyer, T.
AU - Brondum-Nielsen, K.
AU - Tommerup, Niels
AU - Ropers, H.H.
AU - Tümer, Zeynep
AU - Kalscheuer, V.M.
AU - Thomas, N.S.
PY - 2006
Y1 - 2006
N2 - Udgivelsesdato: 2006/5
AB - Udgivelsesdato: 2006/5
M3 - Journal article
VL - 78
SP - 878
EP - 883
JO - American Journal of Human Genetics
JF - American Journal of Human Genetics
SN - 0002-9297
IS - 5
ER -
