Zobrazeno 1 - 10
of 866
pro vyhledávání: '"M. A. Partington"'
Autor:
P. Copestake, M. A. Partington
Publikováno v:
Geological Society, London, Memoirs. 59
This volume provides a landmark documentation of Jurassic sequence stratigraphy in the North Sea Basin, onshore UK and adjacent regions of the British Isles. It includes detailed sequence descriptions, historical syntheses and updated lithostratigrap
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Publikováno v:
Developmental Medicine & Child Neurology. 15:616-627
SUMMARY Whole blood serotonin levels were measured in 83 children with severe mental retardation. Nearly 50 per cent had hyperserotoninaemia (defined as blood serotonin levels over 350ng/ml—the 90th percentile for normal children of similar age). B
Autor:
M. W. Partington
Publikováno v:
Clinical Genetics. 29:151-156
A family is described with a syndrome of short stature, abnormal pigmentation of the skin and mild facial dysmorphism. The short stature and pigmentary anomalies were more marked in the males than the females. The pattern of inheritance appeared X-li
Autor:
M. W. Partington
Publikováno v:
American Journal of Medical Genetics. 37:65-68
Eighteen patients with a diagnosis of the Rubinstein-Taybi syndrome (RTS) 18 to 23 years ago were traced and the survivors were seen personally. The diagnosis was confirmed in 11 patients. Three of these, all women, had died (ages 9, 37, and 52 years
Publikováno v:
Journal of Medical Genetics. 34:719-728
Three families are reported who have a translocation involving 4p16.3. Nine subjects are described with the clinical features of the Pitt-Rogers-Danks (PRD) syndrome confirming pre- and postnatal growth failure, microcephaly, severe mental retardatio
Autor:
P. W. Colley, M. J. Edwards, J. Roberts, John C. Mulley, C. J. Challinor, G. E. Hollway, H. Kozman, M. W. Partington
Publikováno v:
American Journal of Medical Genetics. 53:65-71
Simple ectopia lentis (EL) was studied in a large family, by clinical examination and analysis of linkage to markers in the region of FBN1, the gene for fibrillin which causes Marfan syndrome on chromosome 15. No patient had clinical or echocardiogra
Publikováno v:
Geological Society, London, Petroleum Geology Conference Series. 4:347-370
Sediments of Kimmeridgian to Late Ryazanian age form a group of key hydrocarbon play fairways in the syn-rift Jurassic of the North Sea. The perceived yet-to-find reserves of these often subtle plays, lying at or below seismic resolution, have attrac
Publikováno v:
Geological Society, London, Petroleum Geology Conference Series. 4:371-386
Thirty-three regionally correlatable marine condensed sections containing maximum flooding surfaces have been recognized in the area allowing the North Sea Jurassic succession to be subdivided into 32 genetic stratigraphic sequences ( sensu Galloway)
Autor:
John R. Underhill, M A Partington
Publikováno v:
Geological Society, London, Petroleum Geology Conference Series. 4:337-345
Although the ‘Mid-Cimmerian event’ or unconformity has been recognized over much of Europe, its exact stratigraphic relations and causal mechanism have remained unclear. Application of a genetic sequence stratigraphic approach (using 17 marine co