Genotype and phenotype in 12 additional individuals with SATB2‐associated syndrome
Zarate, Y.A., Kalsner, L., Basinger, A., Jones, J.R., Li, C., Szybowska, M., Xu, Z.L., Vergano, S., Caffrey, A.R., Gonzalez, C.V., Dubbs, H., Zackai, E., Millan, F., Telegrafi, A., Baskin, B., Person, R., Fish, J.L., Everman, D.B.
Published in Clinical genetics (01.10.2017)
Published in Clinical genetics (01.10.2017)
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Journal Article
Parental-reported neurodevelopmental issues in Loeys-Dietz syndrome
Collins, R.T., Flor, J.M., Tang, X., Bange, J.M., Zarate, Y.A.
Published in Research in developmental disabilities (01.12.2018)
Published in Research in developmental disabilities (01.12.2018)
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Journal Article
Bone health and SATB2‐associated syndrome
Zarate, Y.A., Steinraths, M., Matthews, A., Smith, W.E., Sun, A., Wilson, L.C., Brain, C., Allgove, J., Jacobs, B., Fish, J.L., Powell, C.M., Wasserman, W.W., van Karnebeek, C.D., Wakeling, E.L., Ma, N.S.
Published in Clinical genetics (01.03.2018)
Published in Clinical genetics (01.03.2018)
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Journal Article
Additional de novo missense genetic variants in NALCN associated with CLIFAHDD syndrome
Vivero, M., Cho, M.T., Begtrup, A., Wentzensen, I.M., Walsh, L., Payne, K., Zarate, Y.A., Bosanko, K., Schaefer, G.B., DeBrosse, S., Pollack, L., Mason, K., Retterer, K., DeWard, S., Juusola, J., Chung, W.K.
Published in Clinical genetics (01.06.2017)
Published in Clinical genetics (01.06.2017)
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Journal Article