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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

4. A diagnostic challenge of KIT p.V559D and BRAF p.G469A mutations in a paragastric mass.

5. Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers

7. Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

10. PEDIA: prioritization of exome data by image analysis

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

14. Uncovering the contribution of moderate-penetrance susceptibility genes to breast cancer by whole-exome sequencing and targeted enrichment sequencing of candidate genes in women of European ancestry

23. Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders

24. Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndrome

25. Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

26. Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

27. The Interaction of BMP2‐Induced Defect Healing in Rat and Fixator Stiffness Modulates Matrix Alignment and Contraction

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

33. Novel variants in TECRL cause recessive inherited CPVT type 3 with severe and variable clinical symptoms

34. Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

36. Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

38. Impaired proteoglycan glycosylation, elevated TGF-β signaling, and abnormal osteoblast differentiation as the basis for bone fragility in a mouse model for gerodermia osteodysplastica

39. Composite transcriptome assembly of RNA-seq data in a sheep model for delayed bone healing

40. Globale Genexpressionsanalyse der atrophen Pseudarthrose der Ratte

41. A novel mutation in CDH11, encoding cadherin‐11, cause Branchioskeletogenital (Elsahy‐Waters) syndrome

43. Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1and BRCA2pathogenic variants

46. Double NF1 Inactivation Affects Adrenocortical Function in NF1Prx1 Mice and a Human Patient

47. Deletions of chromosomal regulatory boundaries are associated with congenital disease

48. Severe congenital cutis laxa with cardiovascular manifestations due to homozygous deletions in ALDH18A1

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