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Download Aufklarer vol.1 Luftwaffe reconnaisance aircraft units by David Wadman PDF

By David Wadman

Серия «Luftwaffe colors» издательства «Classic courses» посвящена краткой, но очень яркой истории ВВС Третьего рейха. Прекрасно иллюстрированный полный исторический обзор Люфтваффе 1933-1945гг. Авторы серии собрали большое количество редких цветных и ч/б фотографий. Особенно полезна эта серия будет для моделистов (в книгах дается большое количество цветных схем окраски вместе с фотографиями самолетов). В данной книге рассматриваются самолеты-разведчики.

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Dissection of epistasis in oligogenic Bardet-Biedl syndrome. Nature. 2006;439:326–30. Klein RJ, Zeiss C, Chew EY, et al. Complement factor H polymorphism in age-related macular degeneration. Science. 2005;308:385–9. Edwards AO, Ritter R 3rd, Abel KJ, et al. Complement ­factor H polymorphism and age-related macular ­degeneration. Science. 2005;308:421–4. Haines JL, Hauser MA, Schmidt S, et al. Complement factor H variant increases the risk of age-related macular degeneration. Science. 2005;308:419–21.

A fundus dystrophy with unusual features (late onset and dominant inheritance of a central retinal lesion showing oedema, haemorrhage and exudates developing into generalized choroidal atrophy with massive pigment proliferation). Br J Ophthalmol. 1949;33:67–97. Weber GHF, Vogt G, Pruett RC, et al. Mutations in the tissue inhibitor metalloproteinase-3 (TIMP-3) in patients with Sorsby’s fundus dystrophy. Nat Genet. 1994;8: 352–6. Li Z, Clarke MP, Barker MD, McKie N. TIMP3 mutation in Sorsby’s fundus dystrophy: molecular insights.

DNA sequencing can also be performed on specially designed chips. Specific oligonucleotide sequencing primers are normal sequence and all possible mutations are used to construct the chip. Mutation Validation Novel DNA sequence changes are frequently found as a result of direct sequencing. These changes have not been previously associated with a disease phenotype, and they could be benign polymorphisms or causative mutations. Additional studies must be done before the sequence change can be designated as disease causing.

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