Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Peter Heutink"'
Autor:
Marijke J. van Baren, Sumi Chakraverty, Erwin Wauters, Henry Houlden, Ben A. Oostra, Matt Baker, Mike Hutton, Alison Goate, Volker Nowotny, Jennifer M. Kwon, Susanne Froelich, Patrizia Rizzu, Corinne Lendon, John Hardy, Lars Lannfelt, Peter Heutink, Adrian M. Isaacs, Petra Nowotny
Publikováno v:
Genomics, 60, 129-136. Academic Press
Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) is an autosomal dominant condition clinically characterized by behavioral, cognitive, and motor disturbances. Until now, at least 13 different FTDP-17 families that show linka
Autor:
Stephen W. Scherer, Cathleen Berglund, Marijke J. van Baren, Helen Donnis-Keller, Guido J. Breedveld, Andrea K. Burgess, Anne Hing, Ben A. Oostra, Johanna M. Rommens, Marijke Joosse, J. Zguricas, Henk C. Heus, J. C. Wang, Peter Heutink
Publikováno v:
Genomics, 57, 342-351. Academic Press
Preaxial polydactyly is a congenital hand malformation that includes duplicated thumbs, various forms of triphalangeal thumbs, and duplications of the index finger. A locus for preaxial polydactyly has been mapped to a region of 1.9 cM on chromosome
Autor:
Nick A. van Biezen, Ben A. Oostra, Ronald H. Lekanne Deprez, Ad Geurts van Kessel, Ellen C. Zwarthoff, Abel Thijs, Peter Heutink
Publikováno v:
Genomics. 15(1)
Twenty-five single-copy anonymous DNA markers for human chromosome 22 were isolated. These markers were assigned to four different regions on the chromosome. Six markers recognize restriction fragment length polymorphisms. The relative positions of f