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Your search keyword '"Danyel, Magdalena"' showing total 34 results

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34 results on '"Danyel, Magdalena"'

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1. Efficiency of Computer-Aided Facial Phenotyping (DeepGestalt) in Individuals With and Without a Genetic Syndrome: Diagnostic Accuracy Study

2. Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings

5. Broadening the phenotypic and molecular spectrum of FINCA syndrome: Biallelic NHLRC2 variants in 15 novel individuals

6. GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases

7. GestaltMatcher facilitates rare disease matching using facial phenotype descriptors

8. REEV: review, evaluate and explain variants

10. GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases

12. PEDIA: prioritization of exome data by image analysis

14. Three-Dimensional Histological Characterization of the Placental Vasculature Using Light Sheet Microscopy

16. Next-generation phenotyping integrated in a national framework for patients with ultra-rare disorders improves genetic diagnostics and yields new molecular findings

17. Biallelic known and novel DCDC2 variants in cholestatic liver disease: Phenotype–genotype observations in four children

18. Case report: KPTN gene-related syndrome associated with a spectrum of neurodevelopmental anomalies including severe epilepsy

21. FINCA syndrome beyond pulmonary affection: biallelic NHLRC2 variants in eight families with intellectual disability and epilepsy

23. Broadening the phenotypic and molecular spectrum of FINCA syndrome: Biallelic NHLRC2variants in 15 novel individuals

24. CADA: phenotype-driven gene prioritization based on a case-enriched knowledge graph

26. GestaltMatcher: Overcoming the limits of rare disease matching using facial phenotypic descriptors

27. GestaltMatcher: Overcoming the limits of rare disease matching using facial phenotypic descriptors

28. Efficiency of Computer-Aided Facial Phenotyping (DeepGestalt) in Individuals With and Without a Genetic Syndrome: Diagnostic Accuracy Study (Preprint)

29. Additional file 1: of Familial Xp11.22 microdeletion including SHROOM4 and CLCN5 is associated with intellectual disability, short stature, microcephaly and Dent disease: a case report

30. PEDIA:prioritization of exome data by image analysis

33. Autosomal dominant Robinow syndrome associated with a novel <italic>DVL3</italic> splice mutation.

34. GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases.

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