98 results on '"Peters, Hartmut"'
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52. Somali Current rings in the eastern Gulf of Aden
53. Bottom Layer Turbulence in the Red Sea Outflow Plume
54. Comparative Proteomics in Neurodegenerative and Non-neurodegenerative Diseases Suggest Nodal Point Proteins in Regulatory Networking
55. Equilibration and Circulation of Red Sea Outflow Water in the Western Gulf of Aden*
56. Fibrodisplasia osea familiar. Querubismo
57. Mixing and Entrainment in the Red Sea Outflow Plume. Part II: Turbulence Characteristics
58. Mixing and Entrainment in the Red Sea Outflow Plume. Part I: Plume Structure
59. Reply
60. Turbulence Closure, Steady State, and Collapse into Waves
61. Broadly Distributed and Locally Enhanced Turbulent Mixing in a Tidal Estuary
62. Turbulent Mixing in the Red Sea Outflow Plume from a High-Resolution Nonhydrostatic Model
63. Trinucleotide repeat expansions in the junctophilin‐3 gene are not found in caucasian patients with a huntington's disease‐like phenotype
64. Mutations in the gene encoding c-Abl-binding protein SH3BP2 cause cherubism
65. Microstructure Observations of Turbulent Mixing in a Partially Mixed Estuary. Part II: Salt Flux and Stress
66. Microstructure Observations of Turbulent Mixing in a Partially Mixed Estuary. Part I: Dissipation Rate
67. Second-moment closures and length scales for weakly stratified turbulent shear flows
68. Craniosynostosis in cherubism
69. Two independent mutations in a family with neurofibromatosis type 1 (NF1)
70. A novel mutation L1425p in the GAP-region of the NF1 gene detected by temperature gradient gel electrophoresis (TGGE);
71. 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
72. A novel 5-bp deletion in exon 30 of the neurofibromatosis type 1 (NF1) gene
73. A rapid screening for steroid 21-hydroxylase mutations in patients with congenital adrenal hyperplasia
74. On the parameterization of equatorial turbulence: Effect of fine-scale variations below the range of the diurnal cycle
75. Detail and scaling of turbulent overturns in the Pacific Equatorial Undercurrent
76. The diurnal cycle of the upper equatorial ocean: Turbulence, fine-scale shear, and mean shear
77. Diurnal Cycle of Internal Wave Variability in the Equatorial Pacific Ocean: Results from Moored Observations
78. Differential MSH2 promoter methylation in blood cells of Neurofibromatosis type 1 (NF1) patients.
79. Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome.
80. Equatorial and off-equatorial fine-scale and large-scale shear variability at 140°W
81. Gulf of Aden eddies and their impact on Red Sea Water.
82. Very High-Frequency Radar Mapping of Surface Currents.
83. Selective disactivation of neurofibromin GAP activity in neurofibromatosis type 1 (NF1).
84. Robinow syndrome: Phenotypic variability in a family with a novel intragenic ROR2 mutation
85. VHF radar detects oceanic submesoscale vortex along Florida Coast.
86. A compilation of current, temperature and conductivity data from moorings F1 and F2 in the GATE-C-Area
87. GATE : Oceanographic activities on F.R.G. research vessels
88. Zur Kinematik eines stochastischen Feldes interner Wellen in einer Scherströmung
89. Zur Kinematik eines stochastischen Feldes interner Wellen in einer Scherströmung
90. GATE : CTD Data measured on the F.R.G. Ships Shipboard Operations - Calibration - Editing
91. A compilation of CTD- and profiling current meter data from GATE 1974, F.S. 'Meteor' and W.F.S. 'Planet'
92. The kinematics of a stochastic field of internal waves modified by a mean shear current
93. Upper Ocean Shear and Density Variability at the Equator during TROPIC HEAT
94. Hay-Wells-Syndrom bei einem Kind mit Mutation auf dem Gen TP73L.
95. Trinucleotide repeat expansions in the junctophilin‐3gene are not found in caucasian patients with a huntington's disease‐like phenotype
96. 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.
97. Hay-Wells syndrome in a child with mutation in the TP73L gene.
98. Endocrinological and genetic studies in patients with Polycystic Ovary Syndrome (PCOS).
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