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2. De novo terminal deletion of chromosome 15q26.1 characterised by comparative genomic hybridisation and FISH with locus specific probes. Issue 9 (1st September 2001)

3. Delineation of a complex karyotypic rearrangement by microdissection and CGH in a family affected with split foot. Issue 6 (1st June 2000)

4. Familial Cerebellar Ataxia and Amyotrophic Lateral Sclerosis/Frontotemporal Dementia with DAB1 and C9ORF72 Repeat Expansions: An 18‐Year Study. Issue 12 (23rd September 2022)

5. Reflecting on Earlier Experiences with Unsolicited Findings: Points to Consider for Next‐Generation Sequencing and Informed Consent in Diagnostics. Issue 10 (16th July 2013)