Clinical features and molecular genetic analysis in a Turkish family with oral white sponge nevus

by Ak, G., Cassidy, A.J, Çefle, K., Güllüoğlu, M.G, Koray, M., Kürklü, E., McLean, W.-H.-I, Öztürk, Ş, Palandüz, Ş, Tanyeri, H.
Published 2018

Clinical and molecular genetic analysis of a Chinese family with hereditary elliptocytosis caused by a novel mutation in the EPB41 gene

by Cao, M., Huang, Z., Lin, J., Zhang, D., Zhou, H.
Published 2021

Rare and Common Variants Conferring Risk of Tooth Agenesis

by Alonso, I., Audolfsson, G., Bjornsdottir, G., Dhamo, B., Feenstra, B., Geller, F., Gudbjartsson, D.F, Gudmundsson, L., Gustafsson, O., Howe, B.J, Ingason, A., Jonsson, L., Jonsson, R., Jonsson, T., Leslie, E.J, Magnusson, T.E, Marazita, M.L, Melbye, M., Moreno Uribe, L.M, Nawaz, M.S, Nohr, E.A, Oddsson, A., Olafsson, S., Ongkosuwito, E.M, Pinho, T., Rivadeneira, F., Santos, M., Stefansson, H., Stefansson, K., Steinberg, S., Thordarson, A., Unnsteinsdottir, U., Vucic, S., Walters, G.B, Wolvius, E.B, Zervas, M.
Published 2018

Born to cry: A genetic dissection of infant vocalization

by Ashbrook, D.G, Clifford, B.G, Heck, D.H, Lu, L., Riede, T., Roy, S., Scattoni, M.L, Williams, R.W
Published 2018

Molecular cytogenetic studies of a male carrier with a unique (Y;14) translocation: Case report

by Chen, S., Jiang, Y., Li, L., Liu, R., Xi, Q., Zhang, H., Zhang, X.
Published 2021

Circular RNA hsa_circ_0001874 is an indicator for gastric cancer

by Qi, C., Xi, M., Ye, G., Ye, Q.
Published 2021

Functional characterisation of the amyotrophic lateral sclerosis risk locus GPX3/TNIP1

by Bye, C.R, Cheng, F.-F, Garton, F.C, Giacomotto, J., Gusev, A., Henders, A.K, Henderson, R.D, Kabashi, E., Kiernan, M.C, Mathers, S., McCombe, P.A, McRae, A.F, Nabais, M.F, Needham, M., Ngo, S.T, Ophoff, R., Qi, T., Restuadi, R., Schultz, D., Steyn, F.J, Thompson, M.J, Turner, B.J, van den Berg, L.H, van Rheenen, W., Veldink, J.H, Wallace, L., Wray, N.R, Wu, Y., Zaitlen, N., Ziser, L.
Published 2022

Azacitidine regulates DNA methylation of GADD45γ in myelodysplastic syndromes

by Geng, Y., Li, D., Li, J., Liu, L., Yang, Y.
Published 2021

Development of thalamus mediates paternal age effect on offspring reading: A preliminary investigation

by Hancock, R., Hoeft, F., Vandermosten, M., Wang, C., Xia, Z.
Published 2021

Sporadic Pseudohypoparathyroidism Type 1B in Monozygotic Twins: Insights into the Pathogenesis of Methylation Defects

by Bastepe, M., Hamasaki, A., Honjo, S., Iwasaki, K., Iwasaki, Y., Keidai, Y.
Published 2022

Genetic analysis of 39 erythrocytosis and hereditary hemochromatosis-associated genes in the Slovenian family with idiopathic erythrocytosis

by Anžej Doma, S., Debeljak, N., Fink, M., Gašperšič, J., Količ, R., Kristan, A., Kunej, T., Pajič, T., Podgornik, H., Preložnik Zupan, I., Režen, T., Vuga, A., Žula, Š
Published 2021