Haplotype sharing test maps genes for familial cardiomyopathies(†)

P.A. van der Zwaag; J.P. van Tintelen; F. Gerbens; J.D. Jongbloed; L.G. Boven; J.J. van der Smagt; W.P. Roest; I.M. van Langen; H. Bikker; R.N.W. Hauer; M.P. van den Berg; R.M. Hofstra; G.J. Meerman

doi:10.1111/j.1399-0004.2010.01472.x

Haplotype sharing test maps genes for familial cardiomyopathies(†)

Translated title of the contribution: Haplotype sharing test maps genes for familial cardiomyopathies(†)

P.A. van der Zwaag
, J.P. van Tintelen
, F. Gerbens
, J.D. Jongbloed
, L.G. Boven
, J.J. van der Smagt
, W.P. Roest
, I.M. van Langen
, H. Bikker
, R.N.W. Hauer
, M.P. van den Berg
, R.M. Hofstra
, G.J. Meerman

Research output: Contribution to journal › Article › Academic › peer-review

Translated title of the contribution	Haplotype sharing test maps genes for familial cardiomyopathies(†)
Original language	Undefined/Unknown
Pages (from-to)	459-467
Number of pages	9
Journal	Clinical Genetics
Volume	79
Issue number	5
DOIs	https://doi.org/10.1111/j.1399-0004.2010.01472.x
Publication status	Published - 2011

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10.1111/j.1399-0004.2010.01472.x

Cite this

van der Zwaag, P. A., van Tintelen, J. P., Gerbens, F., Jongbloed, J. D., Boven, L. G., van der Smagt, J. J., Roest, W. P., van Langen, I. M., Bikker, H., Hauer, R. N. W., van den Berg, M. P., Hofstra, R. M., & Meerman, G. J. (2011). Haplotype sharing test maps genes for familial cardiomyopathies(†). Clinical Genetics, 79(5), 459-467. https://doi.org/10.1111/j.1399-0004.2010.01472.x

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year = "2011",

doi = "10.1111/j.1399-0004.2010.01472.x",

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T1 - Haplotype sharing test maps genes for familial cardiomyopathies(†)

AU - van der Zwaag, P.A.

AU - van Tintelen, J.P.

AU - Gerbens, F.

AU - Jongbloed, J.D.

AU - Boven, L.G.

AU - van der Smagt, J.J.

AU - Roest, W.P.

AU - van Langen, I.M.

AU - Bikker, H.

AU - Hauer, R.N.W.

AU - van den Berg, M.P.

AU - Hofstra, R.M.

AU - Meerman, G.J.

PY - 2011

Y1 - 2011

U2 - 10.1111/j.1399-0004.2010.01472.x

DO - 10.1111/j.1399-0004.2010.01472.x

M3 - Article

C2 - 20573160

SN - 0009-9163

VL - 79

SP - 459

EP - 467

JO - Clinical Genetics

JF - Clinical Genetics

IS - 5

ER -