45 results on '"Peters, Hartmut"'
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2. Turbulence and high-frequency variability in a deep gravity current outflow.
3. Monozygotic twins with neurofibromatosis type 1 (NF1) display differences in methylation of NF1 gene promoter elements, 5' untranslated region, exon and intron 1.
4. Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia.
5. Differential MSH2 promoter methylation in blood cells of Neurofibromatosis type 1 (NF1) patients.
6. Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome.
7. Missense mutations in the forkhead domain of FOXL2 lead to subcellular mislocalization, protein aggregation and impaired transactivation.
8. Congenital central hypoventilation syndrome with hyperinsulinism in a preterm infant.
9. Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome in a Girl with Chromosome Translocation t(2;3)(q33;q23).
10. Numerical Simulation of the Red Sea Outflow Using HYCOM and Comparison with REDSOX Observations.
11. Hay-Wells syndrome in a child with mutation in the TP73L gene.
12. Turbulence in the wintertime northern Adriatic Sea under strong atmospheric forcing.
13. Bottom Layer Turbulence in the Red Sea Outflow Plume.
14. Somali Current rings in the eastern Gulf of Aden.
15. Equilibration and Circulation of Red Sea Outflow Water in the Western Gulf of Aden.
16. Mutation analysis of BRCA1 and BRCA2 genes in Iranian high risk breast cancer families.
17. Mixing and Entrainment in the Red Sea Outflow Plume. Part I: Plume Structure.
18. Mixing and Entrainment in the Red Sea Outflow Plume. Part II: Turbulence Characteristics.
19. Turbulence Closure, Steady State, and Collapse into Waves.
20. Broadly Distributed and Locally Enhanced Turbulent Mixing in a Tidal Estuary.
21. Turbulent Mixing in the Red Sea Outflow Plume from a High-Resolution Nonhydrostatic Model.
22. Gulf of Aden eddies and their impact on Red Sea Water.
23. Very High-Frequency Radar Mapping of Surface Currents.
24. Microdeletion in the FMR-1 gene: an apparent null allele using routine clinical PCR amplification.
25. Microstructure Observations of Turbulent Mixing in a Partially Mixed Estuary. Part II: Salt Flux and Stress.
26. Second-moment closures and length scales for weakly stratified turbulent shear flows.
27. Two recurrent nonsense mutations and a 4 bp deletion in a quasi-symmetric element in exon 37 of the NF1 gene.
28. Selective disactivation of neurofibromin GAP activity in neurofibromatosis type 1 (NF1).
29. Detail and scaling of turbulent overturns in the Pacific Equatorial Undercurrent.
30. On the parameterization of equatorial turbulence: Effect of fine-scale variations below the range of the diurnal cycle.
31. The diurnal cycle of the upper equatorial ocean: Turbulence, fine-scale shear, and mean shear.
32. Equatorial and off-equatorial fine-scale and large-scale shear variability at 140°W.
33. VHF radar detects oceanic submesoscale vortex along Florida Coast.
34. Ectodermal Defects and Anal Atresia in a Child with a TP63 Mutation-Expanding the Phenotypic Spectrum.
35. Mutations in the gene encoding c-Abl-binding protein SH3BP2 cause cherubism.
36. Differential MSH2 promoter methylation in blood cells of Neurofibromatosis type 1 (NF1) patients.
37. Hay-Wells-Syndrom bei einem Kind mit Mutation auf dem Gen TP73L.
38. CORRIGENDUM.
39. Correction to 'Turbulence in the wintertime northern Adriatic Sea under strong atmospheric forcing'.
40. Reply.
41. Trinucleotide repeat expansions in the junctophilin-3 gene are not found in caucasian patients with a huntington's disease-like phenotype.
42. A rapid screening for steroid 21-hydroxylase mutations in patients with congenital adrenal hyperplasia.
43. A novel mutation L1425p in the GAP-region of the NF1 gene detected by temperature gradient gel electrophoresis (TGGE);.
44. Mutation screening of neurofibromatosis type 1 (NF1) exons 28 and 29 with single strand conformation polymorphism (SSCP): Five novel mutations, one recurrent transition and two polymorphisms in a panel of 118 unrelated NF1 patients.
45. A novel 5-bp deletion in exon 30 of the neurofibromatosis type 1 (NF1) gene.
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