Prenatal genetic testing in 19 fetuses with corpus callosum abnormality

by Peng, C., She, Q., Tan, W., Tang, E., Wang, D., Wang, L.
Published 2021

Genetic analysis and prenatal diagnosis of 20 Chinese families with oculocutaneous albinism

by Li, H., Mao, Y., Tang, S., Xiang, Y., Xu, C., Xu, X., Xu, Y., Zhou, L.
Published 2021

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

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

Association between the TAP1 gene polymorphisms and recurrent respiratory papillomatosis in patients from Western Mexico: A pilot study

by Araujo-Caballero, V., Cazarez-Navarro, G., Govea-Camacho, L.H, Hernandez-Cañaveral, I.I, Martinez-Lopez, E., Muñoz-Valle, J.F, Ortiz-Hernandez, E., Palomares-Marin, J., Rodriguez-Preciado, S.Y
Published 2021

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

Germline variants in DNA repair genes are associated with young-onset head and neck cancer

by Aagaard, M.M, Canto, L.M.D, Chulam, T.C, Cury, S.S, Kowalski, L.P, Marchi, F.A, Miranda, P.M.D, Petersen, A.H, Pinto, C.A.L, Rogatto, S.R
Published 2021

The gene expression of long non-coding RNAs (lncRNAs): MEG3 and H19 in adipose tissues from obese women and its association with insulin resistance and obesity indices

by Akbari Dilmaghani, N., Daneshmoghadam, J., Emamgholipour, S., Karimi, Z., Omidifar, A., shanaki, M.
Published 2021

Heterozygous familial hypercholesterolaemia in a pair of identical twins: A case report and updated review

by Al-Khateeb, A.M, Chua, Y.-A, Mohd Kasim, N.A, Mohd Nawawi, H., Mohd Nor, N.S
Published 2019

Semaphorin-Plexin Signaling: From Axonal Guidance to a New X-Linked Intellectual Disability Syndrome

by Alkhunaizi, E., Brandt, T., Chitayat, D.A, DeFilippo, C.P, Douglas, G.V, Dubbs, H.A, Elloumi, H.Z, Glassford, M.R, Graf, W.D, Hannibal, M.C, Héron, B., Kim, L.E, Marco, E.J, Mignot, C., Monaghan, K.G, Morrow, M.M, Myers, K.A, Parikh, S., Quinonez, S.C, Rajabi, F., Sarnat, H.B, Shankar, S.P, Shinawi, M.S, Steele, J.L, van de Kamp, J.J.P, Veerapandiyan, A., Waldman, A.T
Published 2022

A splicing LMNA mutation causing laminopathies accompanied by aortic valve malformation

by Duan, J., Li, S., Pi, X., Tao, J., Wang, H.
Published 2021

Clinical and biochemical indexes of 11 COVID-19 patients and the genome sequence analysis of the tested SARS-CoV-2

by Huang, Q., Wu, H., Yu, Z., Zhong, Z.
Published 2021

Sensitization profile to sawtooth oak component allergens and their clinical implications

by Jeong, K.Y, Lee, J., Lee, J.-H, Lee, Y.S, Park, J.-W, Park, K.H, Sang, M.K
Published 2021

Duration of viral shedding and culture positivity with postvaccination SARSCoV-2 delta variant infections

by Barczak, A.K, Boucau, J., Chamberlin, G.C, Choudhary, M.C, Flynn, J.P, Gilbert, R.F, Goldstein, R.H, Haneuse, S., Iyer, S., Lemieux, J.E, Li, J.Z, Luu, J., North, C.M, Regan, J., Reynolds, Z., Sacks, C.A, Siedner, M.J, Uddin, R., Vyas, J.M, Vyas, T.
Published 2022

The potential therapeutic role of PTR1 gene in non-healing anthroponotic cutaneous leishmaniasis due to Leishmania tropica

by Bamorovat, M., Davoudi, N., Ghasemi Nejad Almani, P., Kazemi, B., Khosravi, A., Salari, S., Salarkia, E., Sezavar, M., Sharifi, I.
Published 2021

Mitochondrial DNA mutations in Malaysian female breast cancer patients

by Abdullah, M.A, Ahmad, A.F, Ang, G.Y, Baghawi, A., Emran, N.A, Kitan, N., Maniam, S., Omasanggar, R., Teh, L.K, Yu, C.Y
Published 2020

Expression profiling and bioinformatics analysis of exosomal long noncoding RNAs in patients with myasthenia gravis by RNA sequencing

by Chen, T.-T, Lu, W., Lu, Y., Wang, C.-F
Published 2021

A comprehensive expression profile of tRNA-derived fragments in papillary thyroid cancer

by Shan, S., Wang, Y., Zhu, C.
Published 2021

Novel factor VII gene mutations in six families with hereditary coagulation factor VII deficiency

by Fang, Y., Feng, Q., Leng, S., Peng, J., Sheng, Z., Wang, S., Xu, S., Zhang, L., Zhang, X., Zhang, X., Zhang, Y.
Published 2021

A novel COL2A1 mutation causing spondyloepiphyseal dysplasia congenita in a Chinese family

by Cao, X., Chen, Z., Yang, X., Zhao, C., Zhao, J., Zhou, T., Zhou, Y.
Published 2021