Martin-Luther-Universität Halle-Wittenberg

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2006

Turkmen S, Demirhan O, Hoffmann K, Diers A, Zimmer C, Sperling K, Mundlos S.

Cerebellar hypoplasia and quadrupedal locomotion in humans as a recessive trait mapping to chromosome 17p. J Med Genet 43: 461-464, 2006 [PDF   ]


Franke A, Wollstein A, Teuber M, Wittig M, Lu T, Hoffmann K, Nurnberg P, Krawczak M, Schreiber S, Hampe J.

GENOMIZER: an integrated analysis system for genome-wide association data. Hum Mutat 27: 583-588, 2006 [Abstract   ]


Hoffmann K, Müller JS, Stricker S, Megabarne A, Rajab A, Lindner TH, Cohen M, Chouery E, Adaimy L, Ghanem I, Delague V, Boltshauser E, Talim B, Horvath R, Robinson PN, Lochmüller H, Hübner C, Mundlos S.

Escobar syndrome is a prenatal myasthenia caused by disruption of the acetylcholin receptor fetal γ subunit. Am J Hum Genet 79: 303-312, 2006 [PDF   ]


Berger M, Stassen HH, Köhler K, Krane V, Mönks D, Wanner C, Hoffmann K, Hoffmann MM, Zimmer M, Bickeböller H, Lindner TH.

Hidden population substructures in an apparently homogeneous population bias association studies. Eur J Hum Genet 14: 236-244, 2006 [PDF   ]

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