Erratum: Isolated NIPBL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction (European Journal of Human Genetics (2012) 20 (366) DOI:10.1038/ejhg.2011.209)

Diana Braunholz; Melanie Hullings; María Concepcion Gil-Rodríguez; Christopher T. Fincher; Mark B. Mallozzi; Elizabeth Loy; Melanie Albrecht; Maninder Kaur; Janusz Limon; Abhinav Rampuria; Dinah Clark; Antonie Kline; Andreas Dalski; Juliane Eckhold; Andreas Tzschach; Raoul Hennekam; Gabriele Gillessen-Kaesbach; Jolanta Wierzba; Ian D. Krantz; Matthew A. Deardorff; Frank J. Kaiser

doi:10.1038/ejhg.2011.209

Erratum: Isolated NIPBL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction (European Journal of Human Genetics (2012) 20 (366) DOI:10.1038/ejhg.2011.209)

Diana Braunholz, Melanie Hullings, María Concepcion Gil-Rodríguez, Christopher T. Fincher, Mark B. Mallozzi, Elizabeth Loy, Melanie Albrecht, Maninder Kaur, Janusz Limon, Abhinav Rampuria, Dinah Clark, Antonie Kline, Andreas Dalski, Juliane Eckhold, Andreas Tzschach, Raoul Hennekam, Gabriele Gillessen-Kaesbach, Jolanta Wierzba, Ian D. Krantz, Matthew A. DeardorffFrank J. Kaiser

Research output: Contribution to journal › Comment/debate › peer-review

Original language	English (US)
Pages (from-to)	366
Number of pages	1
Journal	European Journal of Human Genetics
Volume	20
Issue number	3
DOIs	https://doi.org/10.1038/ejhg.2011.209
State	Published - Mar 2012
Externally published	Yes

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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10.1038/ejhg.2011.209

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Braunholz, D., Hullings, M., Gil-Rodríguez, M. C., Fincher, C. T., Mallozzi, M. B., Loy, E., Albrecht, M., Kaur, M., Limon, J., Rampuria, A., Clark, D., Kline, A., Dalski, A., Eckhold, J., Tzschach, A., Hennekam, R., Gillessen-Kaesbach, G., Wierzba, J., Krantz, I. D., ... Kaiser, F. J. (2012). Erratum: Isolated NIPBL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction (European Journal of Human Genetics (2012) 20 (366) DOI:10.1038/ejhg.2011.209). European Journal of Human Genetics, 20(3), 366. https://doi.org/10.1038/ejhg.2011.209

Erratum: Isolated NIPBL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction (European Journal of Human Genetics (2012) 20 (366) DOI:10.1038/ejhg.2011.209). / Braunholz, Diana; Hullings, Melanie; Gil-Rodríguez, María Concepcion et al.
In: European Journal of Human Genetics, Vol. 20, No. 3, 03.2012, p. 366.

Research output: Contribution to journal › Comment/debate › peer-review

Braunholz, D, Hullings, M, Gil-Rodríguez, MC, Fincher, CT, Mallozzi, MB, Loy, E, Albrecht, M, Kaur, M, Limon, J, Rampuria, A, Clark, D, Kline, A, Dalski, A, Eckhold, J, Tzschach, A, Hennekam, R, Gillessen-Kaesbach, G, Wierzba, J, Krantz, ID, Deardorff, MA & Kaiser, FJ 2012, 'Erratum: Isolated NIPBL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction (European Journal of Human Genetics (2012) 20 (366) DOI:10.1038/ejhg.2011.209)', European Journal of Human Genetics, vol. 20, no. 3, pp. 366. https://doi.org/10.1038/ejhg.2011.209

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author = "Diana Braunholz and Melanie Hullings and Gil-Rodr{\'i}guez, {Mar{\'i}a Concepcion} and Fincher, {Christopher T.} and Mallozzi, {Mark B.} and Elizabeth Loy and Melanie Albrecht and Maninder Kaur and Janusz Limon and Abhinav Rampuria and Dinah Clark and Antonie Kline and Andreas Dalski and Juliane Eckhold and Andreas Tzschach and Raoul Hennekam and Gabriele Gillessen-Kaesbach and Jolanta Wierzba and Krantz, {Ian D.} and Deardorff, {Matthew A.} and Kaiser, {Frank J.}",

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AU - Gil-Rodríguez, María Concepcion

AU - Fincher, Christopher T.

AU - Mallozzi, Mark B.

AU - Loy, Elizabeth

AU - Albrecht, Melanie

AU - Kaur, Maninder

AU - Limon, Janusz

AU - Rampuria, Abhinav

AU - Clark, Dinah

AU - Kline, Antonie

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AU - Eckhold, Juliane

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AU - Hennekam, Raoul

AU - Gillessen-Kaesbach, Gabriele

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Erratum: Isolated NIPBL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction (European Journal of Human Genetics (2012) 20 (366) DOI:10.1038/ejhg.2011.209)

ASJC Scopus subject areas

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