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41 results on '"Bullich, Gemma"'

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1. Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses

2. ClinPrior: an algorithm for diagnosis and novel gene discovery by network-based prioritization

3. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

4. MYH9 Associated nephropathy

5. Nefropatía asociada a mutación del gen MYH9

6. Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14

7. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

8. Twist exome capture allows for lower average sequence coverage in clinical exome sequencing

9. Twist exome capture allows for lower average sequence coverage in clinical exome sequencing

10. Solving unsolved rare neurological diseases-a Solve-RD viewpoint

11. The RD-connect genome-phenome analysis platform: accelerating diagnosis, research, and gene discovery for rare diseases

12. Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

14. Systematic Collaborative Reanalysis of Genomic Data Improves Diagnostic Yield in Neurologic Rare Diseases

15. The RD‐Connect Genome‐Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases

16. Clinical and Genetic Features of Autosomal Dominant Alport Syndrome: A Cohort Study

17. Clinical and genetic features of autosomal dominant alport syndrome: a case series

18. Solving patients with rare diseases through programmatic reanalysis of genome-phenome data

19. Correction: Solving unsolved rare neurological diseases : A Solve-RD viewpoint

20. Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

21. De Novo PORCN and ZIC2 Mutations in a Highly Consanguineous Family

22. Clinical utility of genetic testing in early-onset kidney disease: seven genes are the main players

23. Clinical utility of genetic testing in early-onset kidney disease: seven genes are the main players.

24. Improved Diagnosis of Rare Disease Patients through Systematic Detection of Runs of Homozygosity

25. Autosomal Dominant Tubulointerstitial Kidney Disease: Clinical Presentation of Patients With ADTKD-UMOD and ADTKD-MUC1

26. A kidney-disease gene panel allows a comprehensive genetic diagnosis of cystic and glomerular inherited kidney diseases

31. Contribution of theTTC21Bgene to glomerular and cystic kidney diseases

32. MYH9Associated nephropathy

34. Targeted next-generation sequencing in steroid-resistant nephrotic syndrome: mutations in multiple glomerular genes may influence disease severity

36. Autosomal Dominant Tubulointerstitial Kidney Disease: Clinical Presentation of Patients With ADTKD-UMODand ADTKD-MUC1

39. Targeted next-generation sequencing in steroid-resistant nephrotic syndrome: mutations in multiple glomerular genes may influence disease severity.

40. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

41. HLA-DQA1 and PLA2R1 polymorphisms and risk of idiopathic membranous nephropathy.

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