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1. Enhancing the analysis of murine neonatal ultrasonic vocalizations: Development, evaluation, and application of different mathematical models

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

5. Benchmarking whole exome sequencing in the German network for personalized medicine

7. O’Donnell-Luria-Rodan syndrome: description of a second multinational cohort and refinement of the phenotypic spectrum

9. NCT/DKFZ MASTER handbook of interpreting whole-genome, transcriptome, and methylome data for precision oncology

11. Public information needs and preferences on COVID-19: a cross-sectional study

12. An analgesic pathway from parvocellular oxytocin neurons to the periaqueductal gray in rats

13. DNA methylation episignature, extension of the clinical features, and comparative epigenomic profiling of Hao-Fountain syndrome caused by variants in USP7

14. Optimal control of colloidal trajectories in inertial microfluidics using the Saffman effect

15. Particle pairs and trains in inertial microfluidics

16. Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain.

19. aRgus: Multilevel visualization of non-synonymous single nucleotide variants & advanced pathogenicity score modeling for genetic vulnerability assessment

20. European Autism GEnomics Registry (EAGER): protocol for a multicentre cohort study and registry

22. Dissipative systems with nonlocal delayed feedback control

23. Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies

25. GestaltMatcher facilitates rare disease matching using facial phenotype descriptors

28. A flowing pair of particles in inertial microfluidics

29. Inertial migration and axial control of deformable capsules

31. Neurocognitive and Neurobehavioral Phenotype of Youth with Schaaf-Yang Syndrome

33. Lösungen

37. Augen

40. Harntrakt

48. MAGEL2 (patho‐)physiology and Schaaf–Yang syndrome.

49. Clinical characterization of int22h1/int22h2-mediated Xq28 duplication/deletion: new cases and literature review

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