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Körpersprachlich Orientierter Fremdsprachenunterricht und Ein Vorführungsversuch Eines Unterrichtsmodells Für Die Deutsche Sprache
(Sosyal Bilimler Enstitüsü, 1997)
Bu araştırmada, yüz yüze yapılan iletişimde,adeta bir örgü gibi bir arada bulunan, dilsel ve dil dışı mesajlardan, dil dışı mesajlar başka bir deyişle beden dili ve nbeden dilinin eğitimindeki yeri, yabancı dil öğrenimine ...
Cerebral Infarct Associated With Factor V Leiden Mutation In A Boy With Hemophilia A
(Wiley-Liss, 1997)
An 11-year-old boy with mild hemophilia A was admitted to our hospital because of focal convulsions, Magnetic resonance imaging showed an old occipital infarct. Protein C, S, antithrombin ill, anticardiolipin antibodies ...
Defects In The E2 Lipoyl Transacetylase And The X-Lipoyl Containing Component Of The Pyruvate-Dehydrogenase Complex In Patients With Lactic Acidemia
(Amer Soc Clinical Investigation Inc, 1990)
Heights And Weights Of Primary School Children Of Different Social Background In Ankara, Turkey
(Oxford Univ Press, 1997)
A cross-sectional anthropometric survey was carried out in a low socio-economic and high socioeconomic region of Ankara, Turkey, to measure the weights and heights of school children, The study group consisted of 5289 ...
Assignment of the Muscle-Eye-Brain Disease Gene to 1P32-P34 by Linkage Analysis and Homozygosity Mapping
(Univ Chicago Press, 1999)
Muscle-eye-brain disease (MEB) is an autosomal recessive disease of unknown etiology characterized by severe mental retardation, ocular abnormalities, congenital muscular dystrophy, and a polymicrogyria-pachygyria-type ...
Calpainopathy - A Survey of Mutations and Polymorphisms
(Cell Press, 1999)
Limb-girdle muscular dystrophy-type 2A (LGMD2A) is an autosomal recessive disorder characterized mainly by symmetrical and selective atrophy of the proximal limb muscles. It derives, from defects in the, human CAPN3 gene, ...
Fish Studies In 45 Patients With Rubinstein-Taybi Syndrome: Deletions Associated With Polysplenia, Hypoplastic Left Heart And Death In Infancy
(Nature Publishing Group, 1999)
Rubinstein-Taybi syndrome (RTS) is a dominant Mendelian disorder characterised by mental retardation, a typical facies, broad thumbs and short stature. Previous reports indicated that 4-25% of RTS patients have a submicroscopic ...
Fukuyama Type Congenital Muscular-Dystrophy In A Turkish Child
(Canadian J Neurol Sci Inc, 1990)
