Breakpoint cloning and haplotype analysis indicate a single origin of the common Inv(10)( p11.2q21.2) mutation among northern Europeans

Mette Gilling; J.S. Dullinger; S. Gesk; S. Metzke-Heidemann; R. Siebert; T. Meyer; K. Brondum-Nielsen; Niels Tommerup; H.H. Ropers; Zeynep Tümer; V.M. Kalscheuer; N.S. Thomas

Breakpoint cloning and haplotype analysis indicate a single origin of the common Inv(10)( p11.2q21.2) mutation among northern Europeans

Mette Gilling, J.S. Dullinger, S. Gesk, S. Metzke-Heidemann, R. Siebert, T. Meyer, K. Brondum-Nielsen, Niels Tommerup, H.H. Ropers, Zeynep Tümer, V.M. Kalscheuer, N.S. Thomas

Research output: Contribution to journal › Journal article › Research › peer-review

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Abstract

Udgivelsesdato: 2006/5

Original language	English
Journal	American Journal of Human Genetics
Volume	78
Issue number	5
Pages (from-to)	878-883
Number of pages	5
ISSN	0002-9297
Publication status	Published - 2006

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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.

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.

In: American Journal of Human Genetics, Vol. 78, No. 5, 2006, p. 878-883.

Research output: Contribution to journal › Journal article › Research › peer-review

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, vol. 78, no. 5, pp. 878-883.

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. In: American Journal of Human Genetics. 2006 ; Vol. 78, No. 5. pp. 878-883.

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