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2. The UK10K project identifies rare variants in health and disease

4. Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis

5. Low-frequency variation in TP53 has large effects on head circumference and intracranial volume

6. Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity

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

8. ECEL1 gene related contractural syndrome: Long-term follow-up and update on clinical and pathological aspects

9. ECEL1 gene related contractural syndrome: Long-term follow-up and update on clinical and pathological aspects

10. Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity

11. Mutations in INPP5K , Encoding a Phosphoinositide 5-Phosphatase, Cause Congenital Muscular Dystrophy with Cataracts and Mild Cognitive Impairment

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

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

14. Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

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

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

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

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

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

20. Bi-allelic mutations in MYL1 cause a severe congenital myopathy.

21. Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling.

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