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6. Tracking the Mediterranean outflow in the Gulf of Cadiz

12. Monozygotic Twins With Neurofibromatosis Type 1 (NF1) Display Differences in Methylation ofNF1Gene Promoter Elements, 5' Untranslated region, Exon and Intron 1

13. Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia

17. Improving Oceanic Overflow Representation in Climate Models: The Gravity Current Entrainment Climate Process Team

20. Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome

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47. Trinucleotide repeat expansions in the junctophilin‐3 gene are not found in caucasian patients with a huntington's disease‐like phenotype

48. Mutations in the gene encoding c-Abl-binding protein SH3BP2 cause cherubism

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