Search

Your search keyword '"Cirak, Sebhattin"' showing total 9 results

Search Constraints

Start Over You searched for: Author "Cirak, Sebhattin" Remove constraint Author: "Cirak, Sebhattin"
9 results on '"Cirak, Sebhattin"'

Search Results

1. Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

2. Whole-genome sequence-based analysis of thyroid function

3. TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport

4. Monoallelic and Biallelic Mutations in MAB21L2 Cause a Spectrum of Major Eye Malformations

5. A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans

6. A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans

7. Whole-genome sequence-based analysis of thyroid function

8. A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans

9. TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport

Catalog

Books, media, physical & digital resources