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

2. Clinical correlation and molecular evaluation confirm that the MLH1 p.Arg182Gly (c.544A>G) mutation is pathogenic and causes Lynch syndrome

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

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

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

10. Unusual presentation of Lynch Syndrome

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

14. Molecular genetic analysis of the 3p — syndrome

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

19. Molecular genetic analysis of the 3p — syndrome

24. Molecular genetic analysis of the 3p — syndrome

28. Molecular genetic analysis of the 3p — syndrome

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