Apparent 15 N uptake kinetics resulting from remineralization1,2
نویسندگان
چکیده
منابع مشابه
Severe phenotype in Angelman syndrome resulting from paternal isochromosome 15.
Angelman syndrome (AS) is a neurogenetic disorder with an occurrence of approximately 1/20 000 live births. Characteristic features include severe mental retardation, absence of speech, seizures, abnormal EEG, hyperactivity, happy disposition with unmotivated laughter, ataxia of gait, and physical anomalies such as microbrachycephaly, macrostomia, protruding tongue, and widely spaced teeth. The...
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ژورنال
عنوان ژورنال: Limnology and Oceanography
سال: 1984
ISSN: 0024-3590
DOI: 10.4319/lo.1984.29.1.0204