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Januar 2000 / Am J Hum Genet A gene for an autosomal dominant scleroatrophic syndrome predisposing to skin cancer (Huriez Syndrome) maps to chromosome 4q23 Y.A. Lee H.P. Stevens E. Delaporte U. Wahn A. Reis 01. Juni 2000 / Am J Hum Genet A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3 R.C. Betz Y.A. Lee A. Bygum F. Brandrup A.I. Bernal J. Toribio J.I. Alvarez G.M. Kukuk H.H.W. Ibsen H.B. Rasmussen T.F. Wienker A. Reis P. Propping R. Kruse S. Cichon M.M. Noethen 01. August 2000 / Am J Hum Genet Localization of a gene for syndactyly type 1 to chromosome 2q34-q36 K. Bosse R.C. Betz Y.A. Lee T.F. Wienker A. Reis H. Kleen P. Propping S. Cichon M.M. Noethen 01. Dezember 2000 / Nat Genet A major susceptibility locus for atopic dermatitis maps to chromosome 3q21 Y.A. Lee U. Wahn R. Kehrt L. Tarani L. Businco D. Gustafsson F. Andersson A.P. Oranje A. Wolkertstorfer A. von Berg U. Hoffmann W. Kuester T.F. Wienker F. Rueschendorf A. Reis 01. Januar 2001 / J Med Genet Localisation of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26 R. Bayoumi K. Saar Y.A. Lee G. Nuernberg A. Reis M. Nur-E-Kamal L.I. Al Gazali Juli 2001 / Nat Genet Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease R.C. Betz B.G.H. Schoser D. Kasper K. Ricker A. Ramirez V. Stein T. Torbergsen Y.A. Lee M.M. Nothen T.F. Wienker J.P. Malin P. Propping A. Reis W. Mortier T.J. Jentsch M. Vorgerd C. Kubisch Dezember 2002 / Biophys Chem Modeling of electrostatic recognition processes in the mammalian mitochondrial steroid hydroxylase system J.J. Mueller A. Lapko K. Ruckpaul U. Heinemann 01. Juni 2003 / Hum Mol Genet Genome-wide linkage reveals a locus for human essential (primary) hypertension on chromosome 12p M. Gong H.Y. Zhang H. Schulz Y.A. Lee K. Sun S. Bähring F.C. Luft P. Nürnberg A. Reis K. Rohde D. Ganten R.T. Hui N. Hübner 01. Januar 2004 / Science A SNP map of the rat genome generated from cDNA sequences H. Zimdahl G. Nyakatura P. Brandt H. Schulz O. Hummel B. Fartmann D. Brett M. Droege J. Monti Y.A. Lee Y.Y. Sun S.Y. Zhao E.E. Winter C.P. Ponting Y. Chen A. Kasprzyk E. Birney D. Ganten N. Hubner Juni 2004 / J Med Genet A fifth locus for otosclerosis, OTSC5, maps to chromosome 3q22-24 K. Van Den Bogaert E.M.R. De Leenheer W. Chen Y. Lee P. Nuernberg R.J.E. Pennings K. Vanderstraeten M. Thys C.W.R.J. Cremers R.J.H. Smith G. Van Camp Seitennummerierung Erste Seite « First Vorherige Seite ‹ Previous … Seite 14 Seite 15 Aktuelle Seite 16 Seite 17 Nächste Seite Next › Letzte Seite Last »
01. Januar 2000 / Am J Hum Genet A gene for an autosomal dominant scleroatrophic syndrome predisposing to skin cancer (Huriez Syndrome) maps to chromosome 4q23 Y.A. Lee H.P. Stevens E. Delaporte U. Wahn A. Reis
01. Juni 2000 / Am J Hum Genet A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3 R.C. Betz Y.A. Lee A. Bygum F. Brandrup A.I. Bernal J. Toribio J.I. Alvarez G.M. Kukuk H.H.W. Ibsen H.B. Rasmussen T.F. Wienker A. Reis P. Propping R. Kruse S. Cichon M.M. Noethen
01. August 2000 / Am J Hum Genet Localization of a gene for syndactyly type 1 to chromosome 2q34-q36 K. Bosse R.C. Betz Y.A. Lee T.F. Wienker A. Reis H. Kleen P. Propping S. Cichon M.M. Noethen
01. Dezember 2000 / Nat Genet A major susceptibility locus for atopic dermatitis maps to chromosome 3q21 Y.A. Lee U. Wahn R. Kehrt L. Tarani L. Businco D. Gustafsson F. Andersson A.P. Oranje A. Wolkertstorfer A. von Berg U. Hoffmann W. Kuester T.F. Wienker F. Rueschendorf A. Reis
01. Januar 2001 / J Med Genet Localisation of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26 R. Bayoumi K. Saar Y.A. Lee G. Nuernberg A. Reis M. Nur-E-Kamal L.I. Al Gazali
Juli 2001 / Nat Genet Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease R.C. Betz B.G.H. Schoser D. Kasper K. Ricker A. Ramirez V. Stein T. Torbergsen Y.A. Lee M.M. Nothen T.F. Wienker J.P. Malin P. Propping A. Reis W. Mortier T.J. Jentsch M. Vorgerd C. Kubisch
Dezember 2002 / Biophys Chem Modeling of electrostatic recognition processes in the mammalian mitochondrial steroid hydroxylase system J.J. Mueller A. Lapko K. Ruckpaul U. Heinemann
01. Juni 2003 / Hum Mol Genet Genome-wide linkage reveals a locus for human essential (primary) hypertension on chromosome 12p M. Gong H.Y. Zhang H. Schulz Y.A. Lee K. Sun S. Bähring F.C. Luft P. Nürnberg A. Reis K. Rohde D. Ganten R.T. Hui N. Hübner
01. Januar 2004 / Science A SNP map of the rat genome generated from cDNA sequences H. Zimdahl G. Nyakatura P. Brandt H. Schulz O. Hummel B. Fartmann D. Brett M. Droege J. Monti Y.A. Lee Y.Y. Sun S.Y. Zhao E.E. Winter C.P. Ponting Y. Chen A. Kasprzyk E. Birney D. Ganten N. Hubner
Juni 2004 / J Med Genet A fifth locus for otosclerosis, OTSC5, maps to chromosome 3q22-24 K. Van Den Bogaert E.M.R. De Leenheer W. Chen Y. Lee P. Nuernberg R.J.E. Pennings K. Vanderstraeten M. Thys C.W.R.J. Cremers R.J.H. Smith G. Van Camp