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Your search keyword '"Pfundt, Rolph"' showing total 30 results

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30 results on '"Pfundt, Rolph"'

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

2. De novo PHF5A variants are associated with craniofacial abnormalities, developmental delay, and hypospadias

3. Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein

4. A Solve-RD ClinVar-based reanalysis of 1,522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

5. Delineation of a KDM2B-related neurodevelopmental disorder and its associated DNA methylation signature

6. DNA methylation episignature for Witteveen-Kolk syndrome due to SIN3A haploinsufficiency

7. Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein

8. Loss-of-function variants in SRRM2 cause a neurodevelopmental disorder

9. Phenotype based prediction of exome sequencing outcome using machine learning for neurodevelopmental disorders

10. Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome

11. Loss-of-function and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct developmental phenotype

12. Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior

13. DLG4-related synaptopathy: a new rare brain disorder

14. Missense variants in ANKRD11cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein

16. De novo CLTC variants are associated with a variable phenotype from mild to severe intellectual disability, microcephaly, hypoplasia of the corpus callosum, and epilepsy

17. CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum

18. Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome

19. The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome

20. Loss-of-function and missense variants in NSD2cause decreased methylation activity and are associated with a distinct developmental phenotype

21. A clinical utility study of exome sequencing versus conventional genetic testing in pediatric neurology

22. Detection of clinically relevant copy-number variants by exome sequencing in a large cohort of genetic disorders

23. De novo CLTCvariants are associated with a variable phenotype from mild to severe intellectual disability, microcephaly, hypoplasia of the corpus callosum, and epilepsy

24. Novel mutations in LRP6 highlight the role of WNT signaling in tooth agenesis

26. Missense variants in ANKRD11cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein

27. De novo PHF5Avariants are associated with craniofacial abnormalities, developmental delay, and hypospadias

28. Novel mutations in LRP6highlight the role of WNT signaling in tooth agenesis

29. Loss-of-function variants in SRRM2cause a neurodevelopmental disorder

30. The ARID1B spectrum in 143 patients

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