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2. Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents. Issue 2 (24th June 2005)

3. Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features. Issue 4 (1st April 2004)

5. The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes. Issue 1 (5th January 2005)

6. Tiling path resolution mapping of constitutional 1p36 deletions by array-CGH: contiguous gene deletion or "deletion with positional effect" syndrome?. Issue 2 (2nd February 2005)