Search Results - "Rensen, Hanneke"

Chromosome 1p21.3 microdeletions comprising DPYD and MIR137 are associated with intellectual disability by Willemsen, Marjolein H, Vallès, Astrid, Kirkels, Laurens A M H, Mastebroek, Mathilde, Olde Loohuis, Nikkie, Kos, Aron, Wissink-Lindhout, Willemijn M, de Brouwer, Arjan P M, Nillesen, Willy M, Pfundt, Rolph, Holder-Espinasse, Muriel, Vallée, Louis, Andrieux, Joris, Coppens-Hofman, Marjolein C, Rensen, Hanneke, Hamel, Ben C J, van Bokhoven, Hans, Aschrafi, Armaz, Kleefstra, Tjitske

“…MicroRNAs (miRNAs) are non-coding gene transcripts involved in post-transcriptional regulation of genes. Recent studies identified miRNAs as important…”
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Further olecular and Clinical Delineation of the Wisconsin Syndrome Phenotype Associated With Interstitial 3q24q25 Deletions by WILLEMSEN, Marjolein H, DE LEEUW, Nicole, FERWERDA, Annemarie, HAMEL, Ben C. J, KLEEFSTRA, Tjitske, MERCER, Catherine, EISENHAUER, Helen, MORRIS, Joanne, COLLINSON, Morag N, BARBER, John C. K, LAM, Stephen T. S, LO, Ivan F. M, RENSEN, Hanneke

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Further molecular and clinical delineation of the Wisconsin syndrome phenotype associated with interstitial 3q24q25 deletions by Willemsen, Marjolein H., de Leeuw, Nicole, Mercer, Catherine, Eisenhauer, Helen, Morris, Joanne, Collinson, Morag N., Barber, John C.K., Lam, Stephen T.S., Lo, Ivan F.M., Rensen, Hanneke, Ferwerda, Annemarie, Hamel, Ben C.J., Kleefstra, Tjitske

“…Deletions of the distal 3q22.3 region encompassing the gene forkhead transcription factor FOXL2 (FOXL2) usually result in intellectual disability (ID) and the…”
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Brief report: effects of fenfluramine on communicative, stereotypic, and inappropriate behaviors of autistic-type mentally handicapped individuals by Duker, P C, Welles, K, Seys, D, Rensen, H, Vis, A, van den Berg, G

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