Menke-Hennekam syndrome 1: A Case Report

por Trusmei, M., Budisteanu, M.
Publicado 2022

Genomic imbalances of chromosome 15 in patients with autistic features and global developmental delay

por Budisteanu, M., Papuc, S., Erbescu, A., Albulescu, L., Arghir, A.
Publicado 2022

Array CGH - A Powerful Tool in Molecular Diagnostic of Pathogenic Microdeletions - Williams-Beuren Syndrome - A Case Report

por STREAȚĂ, I., ȘERBAN-ȘOȘOI, S., BUDIȘTEANU, M., PÎRVU, A., BURADA, F., MIXICH, F., IOANA, M.
Publicado 2016

Floating-Harbor Syndrome: Presentation of The First Romanian Patient with a SRCAP Mutation and Review of The Literature

por Budisteanu, M, Bögershausen, N, Papuc, SM, Moosa, S, Thoenes, M, Riga, D, Arghir, A, Wollnik, B
Publicado 2018

Phenotypic Variability of 17q12 Microdeletion Syndrome – Three Cases and Review of Literature

por Țuțulan-Cuniță, A, Pavel, AG, Dimos, L, Nedelea, M, Ursuleanu, A, Neacșu, AT, Budișteanu, M, Stambouli, D
Publicado 2022

The psychiatric phenotype of 15q11.2-q13.3 duplications

por Budisteanu, M., Papuc, S., Erbescu, A., Andrei, E., Streata, I., Cucu, M., Iliescu, C., Anghelescu, C., Ioana, D., Ioana, M., Rad, F., Arghir, A.
Publicado 2021

Behavior problems associated with brain heterotopia

por Budisteanu, M., Papuc, S., Erbescu, A., Iliescu, C., Dobre, M., Barca, D., Tarta-Arsene, O., Motoescu, C., Dica, A., Sandu, C., Anghelescu, C., Craiu, D., Arghir, A.
Publicado 2021

Multidisciplinary approach in children with autism spectrum disorder

por Stanciu, A.C., Rad, F., Mihailescu, I., Mateescu, L., Grozavescu, R., Andrei, E., Budisteanu, B., Linca, F., Ioana, D., Iliescu, C., Papuc, S., Arghir, A., Dobrescu, I., Budisteanu, M.
Publicado 2021