529 results on '"Blaumeiser A"'
Search Results
2. Population screening for 15q11-q13 duplications: corroboration of the difference in impact between maternally and paternally inherited alleles
3. Thermal Stability and CO Permeability of [C4C1Pyr][NTf2]/Pd(111) Model SCILLs: from UHV to Ambient Pressure
4. The impact of confined placental mosaicism on prenatal cell-free DNA screening: Insights from a monocentric study of 99 cases
5. Multicentric pilot study to standardize clinical whole exome sequencing (WES) for cancer patients
6. Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritance
7. Multicentric pilot study to standardize clinical whole exome sequencing (WES) for cancer patients
8. Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritance
9. OS-025-YI Spatial single-cell profiling and network analysis reveal the immune architecture of hepatocellular carcinoma associated with immune checkpoint inhibitor therapy outcome
10. Tetrasomy 9p, a Prenatal Challenge: Two Novel Cases
11. Children’s group loyalty is related to parental in-group collectivism
12. Chromosomal microarray analysis in prenatal diagnosis : ethical considerations of the Belgian approach
13. Pushing the Limits of Prenatal Ultrasound: A Case of Dorsal Dermal Sinus Associated with an Overt Arnold–Chiari Malformation and a 3q Duplication
14. Outcome of publicly funded nationwide first-tier noninvasive prenatal screening
15. Implementation of Fetal Clinical Exome Sequencing: Comparing Prospective and Retrospective Cohorts
16. Implementation of Exome Sequencing in Prenatal Diagnostics: Chances and Challenges
17. E-book: Verloskunde - Uitgave 2023
18. Terminal deletion of chromosome 13 in a fetus with normal NIPT: The added value of invasive prenatal diagnosis in the NIPT era
19. Phenotypes and genotypes in non‐consanguineous and consanguineous primary microcephaly: High incidence of epilepsy
20. Syntaxin 18 defects in human and zebrafish unravel key roles in early cartilage and bone development
21. A 6-step Approach to Gain Higher Quality Results From Organotypic Hippocampal Brain Slices in a Traumatic Brain Injury Model
22. Genome-Wide MicroRNA Analysis Implicates miR-30b/d in the Etiology of Alopecia Areata
23. Assessment of the Genetic Spectrum of Uncombable Hair Syndrome in a Cohort of 107 Individuals
24. Wilkinson-type catalysts in ionic liquids for hydrogenation of small alkenes: understanding and improving catalyst stability
25. MIRACUM-Pipe: An Adaptable Pipeline for Next-Generation Sequencing Analysis, Reporting, and Visualization for Clinical Decision Making
26. P-718 Preimplantation genetic testing in Belgium: recommendations for the genetic centres
27. Metal–Support Interaction and Charge Distribution in Ceria-Supported Au Particles Exposed to CO
28. MIRACUM-Pipe: An Adaptable Pipeline for Next-Generation Sequencing Analysis, Reporting, and Visualization for Clinical Decision Making
29. Difference in Procedure-Related Risk of Miscarriage between Early and Mid-Trimester Amniocentesis: A Retrospective Cohort Study
30. Population screening for 15q11-q13 duplications: corroboration of the difference in impact between maternally and paternally inherited alleles
31. Implementation of Exome Sequencing in Prenatal Diagnostics: Chances and Challenges
32. Thermal Stability and CO Permeability of [C4C1Pyr][NTf2]/Pd(111) Model SCILLs: from UHV to Ambient Pressure
33. Failed Neuroprotection of Combined Inhibition of L-Type and ASIC1a Calcium Channels with Nimodipine and Amiloride
34. Thermal Stability and CO Permeability of [C4C1Pyr][NTf2]/Pd(111) Model SCILLs: from UHV to Ambient Pressure.
35. Population screening for 15q11-q13 duplications: corroboration of the difference in impact between maternally and paternally inherited alleles
36. Wilkinson-type catalysts in ionic liquids for hydrogenation of small alkenes: understanding and improving catalyst stability
37. Micro-RNA Landscape of Hepatocellular Carcinoma-Derived Extracellular Vesicles
38. Assessment of the Genetic Spectrum of Uncombable Hair Syndrome in a Cohort of 107 Individuals
39. Population screening for 15q11-q13 duplications : corroboration of the difference in impact between maternally and paternally inherited alleles
40. Micro-RNA Landscape of Hepatocellular Carcinoma-Derived Extracellular Vesicles
41. Non‐invasive prenatal testing detects blood chimerism in dizygotic twins
42. Assessment of the Genetic Spectrum of Uncombable Hair Syndrome in a Cohort of 107 Individuals
43. Metal–Support Interaction and Charge Distribution in Ceria-Supported Au Particles Exposed to CO
44. Implementation of genomic arrays in prenatal diagnosis: The Belgian approach to meet the challenges
45. Pushing the Limits of Prenatal Ultrasound: A Case of Dorsal Dermal Sinus Associated with an Overt Arnold–Chiari Malformation and a 3q Duplication
46. CO Permeability and Wetting Behavior of Ionic Liquids on Pt(111): An IRAS and PM-IRAS Study from Ultrahigh Vacuum to Ambient Pressure
47. Outcome of publicly funded nationwide first-tier noninvasive prenatal screening
48. Supraparticles for Bare‐Eye H2 Indication and Monitoring: Design, Working Principle, and Molecular Mobility
49. Prenatale diagnostiek anno 2015
50. Hydrogen Production Based on Liquid Organic Hydrogen Carriers through Sulfur Doped Platinum Catalysts Supported on TiO2
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