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1. A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry

2. Author Correction: A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry

3. Author Correction: Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

4. Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease

6. Genetic variants associated with longitudinal changes in brain structure across the lifespan

7. Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance

8. Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

10. Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease

11. Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease

13. Heterozygous PNPT1 Variants Cause Spinocerebellar Ataxia Type 25

15. Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease

16. Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

17. Pathogenic Variants in GPC4 Cause Keipert Syndrome

19. GPC4 ; Keipert syndrome ; Nasodigitoacoustic syndrome ; glypicans

20. Pathogenic Variants in GPC4 Cause Keipert Syndrome

23. Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance

24. Identifying disease-causing short tandem repeat expansions in massively parallel sequencing data, with a focus on ataxias

25. Identifying disease-causing short tandem repeat expansions in massively parallel sequencing data, with a focus on ataxias

26. Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance.

28. Complete callosal agenesis, pontocerebellar hypoplasia, and axonal neuropathy due to AMPD2 loss

29. PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy

30. Challenges of diagnostic exome sequencing in an inbred founder population

31. Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

32. Dynamics of Brain Structure and its Genetic Architecture over the Lifespan

33. Dynamics of Brain Structure and its Genetic Architecture over the Lifespan

34. Heterozygous mutations in HSD17B4 cause juvenile peroxisomal D-bifunctional protein deficiency.

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