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47 results on '"Havlovicova, M."'

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1. Dental abnormalities observed in the oculo-facio-cardio-dental (OFCD) syndrome present in two Czech families bearing novel de novo BCOR pathogenic variants.

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

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

4. Expanded DMPK repeats in dizygotic twins referred for diagnosis of autism versus absence of expanded DMPK repeats at screening of 330 children with autism

5. Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis (European Journal of Human Genetics, (2021), 29, 9, (1359-1368), 10.1038/s41431-021-00900-2)

6. Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint (European Journal of Human Genetics, (2021), 29, 9, (1332-1336), 10.1038/s41431-021-00901-1)

7. Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

8. Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders (Nature Communications, (2020), 11, 1, (4932), 10.1038/s41467-020-18723-y)

9. Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

10. Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders (Nature Communications, (2020), 11, 1, (4932), 10.1038/s41467-020-18723-y)

11. Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders (vol 11, 4932, 2020)

12. Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

13. De novo SMARCA2 variants clustered outside the helicase domain cause a new recognizable syndrome with intellectual disability and blepharophimosis distinct from Nicolaides–Baraitser syndrome

14. Dominant variants in the splicing factor PUF60 cause a recognizable syndrome with intellectual disability, heart defects and short stature

15. Mapping the gene for Noonan syndrome (NS1) to a 200-kb region on chromosome 12q24.2

16. HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain

21. Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related Autosomal Recessive Ectodermal Dysplasia 14

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

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

24. De novo SMARCA2 variants clustered outside the helicase domain cause a new recognizable syndrome with intellectual disability and blepharophimosis distinct from Nicolaides-Baraitser syndrome

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

26. Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.

27. Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.

28. Assisted Reproductive Techniques and Pregnancy Results in Women with Mayer-Rokitansky-Küster-Hauser Syndrome Undergoing Uterus Transplantation: the Czech Experience.

29. Telemedicine strategy of the European Reference Network ITHACA for the diagnosis and management of patients with rare developmental disorders.

30. Parental gonadal but not somatic mosaicism leading to de novo NFIX variants shared by two brothers with Malan syndrome.

31. De novo mutations in the GTP/GDP-binding region of RALA, a RAS-like small GTPase, cause intellectual disability and developmental delay.

32. Under the mask of Kabuki syndrome: Elucidation of genetic-and phenotypic heterogeneity in patients with Kabuki-like phenotype.

33. FOXP1 -related intellectual disability syndrome: a recognisable entity.

34. Analysis of 31-year-old patient with SYNGAP1 gene defect points to importance of variants in broader splice regions and reveals developmental trajectory of SYNGAP1-associated phenotype: case report.

35. A patient showing features of both SBBYSS and GPS supports the concept of a KAT6B-related disease spectrum, with mutations in mid-exon 18 possibly leading to combined phenotypes.

36. A 15 Mb large paracentric chromosome 21 inversion identified in Czech population through a pair of flanking duplications.

38. The importance of advanced parental age in the origin of neurofibromatosis type 1.

39. Odor detection threshold, but not odor identification, is impaired in children with autism.

40. Brief report: significant differences in perceived odor pleasantness found in children with ASD.

41. FMR1 gene expansion, large deletion of Xp, and skewed X-inactivation in a girl with mental retardation and autism.

42. Highly unstable sequence interruptions of the CTG repeat in the myotonic dystrophy gene.

43. Molecular cloning and analysis of breakpoints on ring chromosome 17 in a patient with autism.

44. A girl with neurofibromatosis type 1, atypical autism and mosaic ring chromosome 17.

45. Prader-Willi syndrome due to uniparental disomy in a patient with a balanced chromosomal translocation.

46. Subtypes of autism by cluster analysis based on structural MRI data.

47. Not EEG abnormalities but epilepsy is associated with autistic regression and mental functioning in childhood autism.

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