A frequent oligogenic involvement in congenital hypothyroidism

T. de Filippis; G. Gelmini; E. Paraboschi; M.C. Vigone; M. Di Frenna; F. Marelli; M. Bonomi; A. Cassio; D. Larizza; M. Moro; G. Radetti; M. Salerno; D. Ardissino; G. Weber; D. Gentilini; F. Guizzardi; S. Duga; L. Persani

doi:10.1093/hmg/ddx145

A frequent oligogenic involvement in congenital hypothyroidism

T. de Filippis, G. Gelmini, E. Paraboschi, M.C. Vigone, M. Di Frenna, F. Marelli, M. Bonomi, A. Cassio, D. Larizza, M. Moro, G. Radetti, M. Salerno, D. Ardissino, G. Weber, D. Gentilini, F. Guizzardi, S. Duga, L. Persani

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

Original language	English
Pages (from-to)	2507-2514
Number of pages	8
Journal	Human Molecular Genetics
Volume	26
Issue number	13
DOIs	https://doi.org/10.1093/hmg/ddx145
Publication status	Published - 2017

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10.1093/hmg/ddx145

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de Filippis, T., Gelmini, G., Paraboschi, E., Vigone, M. C., Di Frenna, M., Marelli, F., Bonomi, M., Cassio, A., Larizza, D., Moro, M., Radetti, G., Salerno, M., Ardissino, D., Weber, G., Gentilini, D., Guizzardi, F., Duga, S., & Persani, L. (2017). A frequent oligogenic involvement in congenital hypothyroidism. Human Molecular Genetics, 26(13), 2507-2514. https://doi.org/10.1093/hmg/ddx145

de Filippis, T, Gelmini, G, Paraboschi, E, Vigone, MC, Di Frenna, M, Marelli, F, Bonomi, M, Cassio, A, Larizza, D , Moro, M, Radetti, G, Salerno, M, Ardissino, D, Weber, G , Gentilini, D , Guizzardi, F , Duga, S & Persani, L 2017, 'A frequent oligogenic involvement in congenital hypothyroidism', Human Molecular Genetics, vol. 26, no. 13, pp. 2507-2514. https://doi.org/10.1093/hmg/ddx145

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title = "A frequent oligogenic involvement in congenital hypothyroidism",

author = "{de Filippis}, T. and G. Gelmini and E. Paraboschi and M.C. Vigone and {Di Frenna}, M. and F. Marelli and M. Bonomi and A. Cassio and D. Larizza and M. Moro and G. Radetti and M. Salerno and D. Ardissino and G. Weber and D. Gentilini and F. Guizzardi and S. Duga and L. Persani",

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doi = "10.1093/hmg/ddx145",

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T1 - A frequent oligogenic involvement in congenital hypothyroidism

AU - de Filippis, T.

AU - Gelmini, G.

AU - Paraboschi, E.

AU - Vigone, M.C.

AU - Di Frenna, M.

AU - Marelli, F.

AU - Bonomi, M.

AU - Cassio, A.

AU - Larizza, D.

AU - Moro, M.

AU - Radetti, G.

AU - Salerno, M.

AU - Ardissino, D.

AU - Weber, G.

AU - Gentilini, D.

AU - Guizzardi, F.

AU - Duga, S.

AU - Persani, L.

N1 - Cited By :1 Export Date: 7 February 2018

PY - 2017

Y1 - 2017

U2 - 10.1093/hmg/ddx145

DO - 10.1093/hmg/ddx145

M3 - Article

VL - 26

SP - 2507

EP - 2514

JO - Human Molecular Genetics

JF - Human Molecular Genetics

SN - 0964-6906

IS - 13

ER -