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You searched for: Author/Creator Finelli, P- Finelli, P [remove] 3
- 616.042 2
- Medical genetics -- Periodicals 2
- 618 1
- BWS, Beckwith-Wiedemann syndrome -- FISH, fluorescent in situ hybridisation -- UPD, uniparental disomy -- WHS, Wolf-Hirschorn syndrome 1
- Beckwith-Wiedemann syndrome -- chromosomal rearrangements -- imprinting 11p15 region -- segmental duplicons 1
- FISH, fluorescence in situ hybridisation 1
- Human reproduction -- Periodicals 1
- autism -- dup(16)(p11.2p12.2) -- duplicons -- FISH 1
- whole-exome sequencing -- primary ovarian insufficiency -- case-control analysis -- Drosophila comparative analysis and modelling -- gene functional categorisation 1