Results 161 to 170 of about 217,051 (354)
Atlas of Mental Retardation Syndromes. Visual Diagnosis of Facies and Physical Findings [PDF]
, 1970 L. T. Hilliard
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Boreas, EarlyView.The last (Wisconsinan) glacial period was punctuated in North America by two glacial maxima, known as the Early and Late Wisconsinan glaciations. In Alaska, these maxima and their subsequent retreats have been the object of dating efforts to reconstruct local climatic events and compare them to global trends.
Bruno Belotti +5 more
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Boreas, EarlyView.Glacial erosion during the Last Glacial Maximum (LGM) has removed much evidence of earlier glaciations and interglacials in the European Alps. At Gröbminger Mitterberg (GM), beneath a blanket of LGM till, a distinctive sediment archive preserves deposits predating the LGM.
Gerit E. U. Griesmeier +7 more
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, 2011 [ES] Definición del término Facie en el diccionario Dicter. [EN] Definition of the word Facie in the dictionary Dicter.
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Boreas, EarlyView.The interaction between glaciers and the debris accumulating on their surfaces is critical as the Earth warms, with consequences for ice dynamics, hydrology and mass balance together with slope and sedimentary processes. Understanding this interaction is necessary since it influences ablation rates, sediment and meltwater pathways.
Paulina Mejías Osorio +5 more
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Cl-rich minerals in Archean granulite facies ironstones from the Beartooth Mountains, Montana, USA: Implications for fluids involved in granulite metamorphism [PDF]
The implications of Cl-rich minerals in granulite facies rocks are discussed. Results from ironstones of the Beartooth Mountains, Montana are discussed. It is suggested that CO2-brine immiscibility might be applicable to granulite facies conditions, and ...
Henry, D. J.
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Clinical Genetics, EarlyView.We present the first published case of HYPK‐related neurodevelopmental disorder in a male proband with atypical facies, developmental delay, and autism spectrum disorder– like features. HYPK is a part of the NatA complex, like NAA10 and NAA15, with dysfunction leading to similar but milder features to those of Ogden Syndrome.
Rahi Patel +10 more
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MAP1B Variants Disrupt Neuronal Migration: Insights From Three Novel Families
Clinical Genetics, EarlyView.Pathogenic variants in MAP1B have recently emerged as a cause of neurodevelopmental disorders characterized by intellectual disability, epilepsy, and cortical malformations, including periventricular nodular heterotopia (PVNH) and polymicrogyria (PMG).
Jessica Archer +4 more
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