214 results on '"Peters, Hartmut"'
Search Results
2. Tracking the Mediterranean outflow in the Gulf of Cadiz
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. IMPROVING OCEANIC OVERFLOW REPRESENTATION IN CLIMATE MODELS : The Gravity Current Entrainment Climate Process Team
5. Ectodermal Defects and Anal Atresia in a Child with a TP63 Mutation-Expanding the Phenotypic Spectrum
6. Pathways of Nordic Overflows from climate model scale and eddy resolving simulations
7. Performance of two-equation turbulence closures in three-dimensional simulations of the Red Sea overflow
8. Very large eddy simulation of the Red Sea overflow
9. Congenital central hypoventilation syndrome with hyperinsulinism in a preterm infant
10. Validating a turbulence closure against estuarine microstructure measurements
11. Mutation analysis of BRCA1 and BRCA2 genes in Iranian high risk breast cancer families
12. Contributors
13. Temperature and Denaturing Gradient Gel Electrophoresis
14. Parameterization of gravity current entrainment for ocean circulation models using a high-order 3D nonhydrostatic spectral element model
15. Deletions of the RUNX2 Gene Are Present in About 10% of Individuals with Cleidocranial Dysplasia
16. Spatial and temporal variability of turbulent mixing in an estuary
17. The gene for cherubism maps to chromosome 4p16
18. A New Autosomal Recessive Syndrome Characterized by Ocular Hypertelorism, Distinctive Face, Mental Retardation, Brachydactyly, and Genital Abnormalities
19. Comparison of gravity current mixing parameterizations and calibration using a high-resolution 3D nonhydrostatic spectral element model
20. Cherubism – new hypotheses on pathogenesis and therapeutic consequences
21. Robinow syndrome: Phenotypic variability in a family with a novel intragenic ROR2 mutation
22. Missense mutations in the forkhead domain of FOXL2 lead to subcellular mislocalization, protein aggregation and impaired transactivation
23. Hay-Wells syndrome in a child with mutation in the TP73L gene
24. Two recurrent nonsense mutations and a 4 bp deletion in a quasi-symmetric element in exon 37 of the NF1 gene
25. Microdeletion in the FMR-1 gene: an apparent null allele using routine clinical PCR amplification
26. Development of a Two-Equation Turbulence Model for Mean Shear- and Internal Wave-Driven Mixing
27. Cruise Report: DOLCE VITA 1 and 2, 31 January-24 February and 26 May-15 June, 2003
28. Diapycnal Mixing in the Strait of Hormuz
29. Two Novel Monoallelic Calreticulin Mutations in a Patient With Essential Thrombocythemia
30. Minor Lesion Mutational Spectrum of the Entire NF1 Gene Does Not Explain Its High Mutability but Points to a Functional Domain Upstream of the GAP-Related Domain
31. Identification of the first multi-exonic WDR72 deletion in isolated amelogenesis imperfecta, and generation of a WDR72-specific copy number screening tool
32. Recurrence of split hand/foot malformation, cleft lip/palate, and severe urogenital abnormalities due to germline mosaicism forTP63mutation
33. Turbulence and high-frequency variability in a deep gravity current outflow
34. Water mass transformation of the Mediterranean outflow West of Gibraltar
35. Topographic steering of the Mediterranean Outflow West of Gibraltar
36. Shallow Water Fronts, River Plumes and Response to Strong Forcing - Preliminary Results from Intensive Surveys of the Northern Adriatic
37. Shallow water fronts, river plumes and strong forcing ; preliminary results from intensive surveys of the northern Adriatic
38. Ectodermal Defects and Anal Atresia in a Child with aTP63Mutation-Expanding the Phenotypic Spectrum
39. Shallow water fronts, river plumes and response to strong forcing – preliminary results from intensive surveys of the northern Adriatic
40. Turbulence and high‐frequency variability in a deep gravity current outflow
41. Monozygotic Twins With Neurofibromatosis Type 1 (NF1) Display Differences in Methylation ofNF1Gene Promoter Elements, 5' Untranslated region, Exon and Intron 1
42. Erratum: Differential MSH2 promoter methylation in blood cells of Neurofibromatosis type 1 (NF1) patients
43. Differential MSH2 promoter methylation in blood cells of Neurofibromatosis type 1 (NF1) patients
44. Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome
45. Numerical Simulation of the Red Sea Outflow Using HYCOM and Comparison with REDSOX Observations
46. Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome in a Girl with Chromosome Translocation t(2;3)(q33;q23)
47. Hay‐Wells syndrome in a child with mutation in the TP73L gene
48. Hay‐Wells‐Syndrom bei einem Kind mit Mutation auf dem Gen TP73L
49. CORRIGENDUM
50. Correction to “Turbulence in the wintertime northern Adriatic Sea under strong atmospheric forcing”
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