Targeted carrier screening for four recessive disorders: High detection rate within a founder population

I.B. Mathijssen; L. Henneman; J.M.C. van Eeten-Nijman; P. Lakeman; C.P.E. Ottenheim; E.J.W. Redeker; W. Ottenhof; H. Meijers-Heijboer; M.C. van Maarle

doi:10.1016/j.ejmg.2015.01.004

Targeted carrier screening for four recessive disorders: High detection rate within a founder population

I.B. Mathijssen, L. Henneman, J.M.C. van Eeten-Nijman, P. Lakeman, C.P.E. Ottenheim, E.J.W. Redeker, W. Ottenhof, H. Meijers-Heijboer, M.C. van Maarle

Clinical genetics

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

Original language	Undefined/Unknown
Pages (from-to)	123-128
Journal	European Journal of Medical Genetics
Volume	58
Issue number	3
DOIs	https://doi.org/10.1016/j.ejmg.2015.01.004
Publication status	Published - 2015

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10.1016/j.ejmg.2015.01.004

Cite this

Mathijssen, I. B., Henneman, L., van Eeten-Nijman, J. M. C., Lakeman, P., Ottenheim, C. P. E., Redeker, E. J. W., Ottenhof, W., Meijers-Heijboer, H., & van Maarle, M. C. (2015). Targeted carrier screening for four recessive disorders: High detection rate within a founder population. European Journal of Medical Genetics, 58(3), 123-128. https://doi.org/10.1016/j.ejmg.2015.01.004

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Targeted carrier screening for four recessive disorders: High detection rate within a founder population. / Mathijssen, I.B.; Henneman, L.; van Eeten-Nijman, J.M.C.; Lakeman, P.; Ottenheim, C.P.E.; Redeker, E.J.W.; Ottenhof, W.; Meijers-Heijboer, H.; van Maarle, M.C.

In: European Journal of Medical Genetics, Vol. 58, No. 3, 2015, p. 123-128.

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

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T1 - Targeted carrier screening for four recessive disorders: High detection rate within a founder population

AU - Mathijssen, I.B.

AU - Henneman, L.

AU - van Eeten-Nijman, J.M.C.

AU - Lakeman, P.

AU - Ottenheim, C.P.E.

AU - Redeker, E.J.W.

AU - Ottenhof, W.

AU - Meijers-Heijboer, H.

AU - van Maarle, M.C.

PY - 2015

Y1 - 2015

U2 - 10.1016/j.ejmg.2015.01.004

DO - 10.1016/j.ejmg.2015.01.004

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VL - 58

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EP - 128

JO - European Journal of Medical Genetics

JF - European Journal of Medical Genetics

SN - 1769-7212

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