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1. Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections

2. Prevalence and architecture of de novo mutations in developmental disorders

3. Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

4. The contribution of X-linked coding variation to severe developmental disorders

5. Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations

7. EFTUD2 haploinsufficiency leads to syndromic oesophageal atresia

8. Clinical and radiological characterization of novel FIG4‐related combined system disease with neuropathy

10. Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes

11. Identification of genetic markers associated with Gilles de la Tourette syndrome in an Afrikaner population

12. CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

13. Haploinsufficiency of CUX1 Causes Nonsyndromic Global Developmental Delay With Possible Catch-up Development

15. Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy

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

17. Method to Synchronize Cell Cycle of Human Pluripotent Stem Cells without Affecting Their Fundamental Characteristics

18. Haploinsufficiency of CUX1 Causes Nonsyndromic Global Developmental Delay With Possible Catch-up Development

19. Reconstruction of the mouse extrahepatic biliary tree using primary human extrahepatic cholangiocyte organoids

20. STAG1 mutations cause a novel cohesinopathy characterised by unspecific syndromic intellectual disability

21. Mutation of the human mitochondrial phenylalanine-tRNA synthetase causes infantile-onset epilepsy and cytochrome c oxidase deficiency

22. Haploinsufficiency of CUX1 Causes Nonsyndromic Global Developmental Delay With Possible Catch‐up Development

23. Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders

24. STAG1 mutations cause a novel cohesinopathy characterised by unspecific syndromic intellectual disability

25. STAG1 mutations cause a novel cohesinopathy characterised by unspecific syndromic intellectual disability

27. STAG1mutations cause a novel cohesinopathy characterised by unspecific syndromic intellectual disability

28. Biallelic CRELD1variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections

29. A novel microdeletion syndrome at 9q21.13 characterised by mental retardation, speech delay, epilepsy and characteristic facial features

30. Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation: The Deciphering Developmental Disorders Study

31. Association of a germline copy number polymorphism of APOBEC3A and APOBEC3B with burden of putative APOBEC-dependent mutations in breast cancer

33. Exonic Deletions in AUTS2 Cause a Syndromic Form of Intellectual Disability and Suggest a Critical Role for the C Terminus

34. EFTUD2haploinsufficiency leads to syndromic oesophageal atresia

43. Novel deletion variants of 9q13–q21.12 and classical euchromatic variants of 9q12/qh involve deletion, duplication and triplication of large tracts of segmentally duplicated pericentromeric euchromatin.

45. Method to Synchronize Cell Cycle of Human Pluripotent Stem Cells without Affecting Their Fundamental Characteristics

46. Association of a germline copy number polymorphism of APOBEC3A and APOBEC3B with burden of putative APOBEC-dependent mutations in breast cancer

47. Reconstruction of the mouse extrahepatic biliary tree using primary human extrahepatic cholangiocyte organoids

48. Reconstruction of the mouse extrahepatic biliary tree using primary human extrahepatic cholangiocyte organoids

49. Reconstruction of the mouse extrahepatic biliary tree using primary human extrahepatic cholangiocyte organoids

50. Reconstruction of the mouse extrahepatic biliary tree using primary human extrahepatic cholangiocyte organoids

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