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You searched for: Author/Creator Melchior, Linea

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1. A mosaic small supernumerary marker chromosome 17 in a patient with Tourette syndrome, ADHD and intellectual disability: A case story and review of the literature. Issue 1 (30th July 2015)

2. A t(3;9)(q25.1;q34.3) translocation leading to OLFM1 fusion transcripts in Gilles de la Tourette syndrome, OCD and ADHD. Issue 3 (28th February 2015)

3. Deletions and rearrangements of the H19/IGF2 enhancer region in patients with Silver–Russell syndrome and growth retardation. Issue 5 (28th January 2011)

4. Increase of Ki‐67 index and influence on mortality in patients with neuroendocrine neoplasms. (19th August 2021)