The eponymous Jacobsen syndrome: mapping the breakpoints of the original family suggests an association between the distal 1.1. Mb of chromosome 21 and osteoporosis in Down syndrome

Zeynep A Tümer; A.M. Henriksen; Iben Bache; Lars Allan Larsen; K. Brixen; N. Illum; K. Rasmussen; Niels Tommerup

The eponymous Jacobsen syndrome: mapping the breakpoints of the original family suggests an association between the distal 1.1. Mb of chromosome 21 and osteoporosis in Down syndrome

Zeynep A Tümer, A.M. Henriksen, Iben Bache, Lars Allan Larsen, K. Brixen, N. Illum, K. Rasmussen, Niels Tommerup

4 Citations (Scopus)

Original language	English
Journal	American Journal of Medical Genetics. Part C: Seminars in Medical Genetics
Issue number	Vol. 135A
Pages (from-to)	339-341
ISSN	1552-4868
Publication status	Published - 2005

Cite this

Tümer, Z. A., Henriksen, A. M., Bache, I., Larsen, L. A., Brixen, K., Illum, N., Rasmussen, K., & Tommerup, N. (2005). The eponymous Jacobsen syndrome: mapping the breakpoints of the original family suggests an association between the distal 1.1. Mb of chromosome 21 and osteoporosis in Down syndrome. American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, (Vol. 135A), 339-341.

The eponymous Jacobsen syndrome: mapping the breakpoints of the original family suggests an association between the distal 1.1. Mb of chromosome 21 and osteoporosis in Down syndrome. / Tümer, Zeynep A; Henriksen, A.M.; Bache, Iben et al.
In: American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, No. Vol. 135A, 2005, p. 339-341.

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

Tümer, ZA, Henriksen, AM, Bache, I , Larsen, LA, Brixen, K, Illum, N, Rasmussen, K & Tommerup, N 2005, 'The eponymous Jacobsen syndrome: mapping the breakpoints of the original family suggests an association between the distal 1.1. Mb of chromosome 21 and osteoporosis in Down syndrome', American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, no. Vol. 135A, pp. 339-341.

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