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Chromosome aberrations involving 10q22: report of three overlapping interstitial deletions and a balanced translocation disrupting C10orf11.
Authors: Tzschach, Andreas; Bisgaard, Anne-Marie; Kirchhoff, Maria; Graul-Neumann, Luitgard M.; Neitzel, Heidemarie; Page, Stephanie; Ahmed, Alischo; Müller, Ines; Erdogan, Fikret; Ropers, Hans-Hilger; Kalscheuer, Vera M.; Ullmann, Reinhard
Date of Publication (YYYY-MM-DD): 2010-03-01
Title of Journal: European Journal of Human Genetics : EJHG
Volume: 18
Issue / Number: 3
Start Page: 291
End Page: 295
Document Type: Article
ID: 536097.0


An integrative approach for analyzing the interplay of genetic and epigenetic changes in tumors
Authors: Muradyan, Artur; Boldt, Vivien; Steininger, Anne; Stabentheiner, Stephanie; Tebel, Katrin; Kreutzberger, Jürgen; Müller, Ines; Madle, Hannelore; Popper, Helmut H.; Ullmann, Reinhard
Date of Publication (YYYY-MM-DD): 2008-10
Title of Journal: Archives of Pathology and Laboratory Medicine
Volume: 132
Issue / Number: 10
Start Page: 1557
End Page: 1561
Document Type: Article
ID: 411051.0


The genome of Erwinia tasmaniensis strain Et1/99, a non-pathogenic bacterium in the genus Erwinia
Authors: Kube, Michael; Migdoll, Alexander Michael; Müller, Ines; Kuhl, Heiner; Beck, Alfred; Reinhardt, Richard; Geider, Klaus
Date of Publication (YYYY-MM-DD): 2008-05-06
Title of Journal: Environmental Microbiology
Volume: 10
Issue / Number: 9
Start Page: 2211
End Page: 2222
Document Type: Article
ID: 416175.0


Diagnosis of a terminal deletion of 4p with duplication of Xp22.31 in a patient with findings of Opitz G/BBB syndrome and Wolf-Hirschhorn syndrome
Authors: So, Joyce; Müller, Ines; Kunath, Melanie; Herrmann, Susanne; Ullmann, Reinhard; Schweiger, Susann
Date of Publication (YYYY-MM-DD): 2008-01
Title of Journal: American Journal of Medical Genetics Part A
Volume: 146A
Issue / Number: 1
Start Page: 103
End Page: 109
Document Type: Article
ID: 411235.0


Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation
Authors: Ullmann, Reinhard; Turner, Gillian; Kirchhoff, Maria; Chen, Wei; Tonge, Bruce; Rosenberg, Carla; Field, Michael; Vianna-Morgante, Angela M.; Christie, Louise; Krepischi-Santos, Ana C.; Banna, Lynn; Brereton, Avril V.; Hill, Alyssa; Bisgaard, Anne-Marie; Müller, Ines; Hultschig, Claus; Erdogan, Fikret; Wieczorek, Georg; Ropers, Hans-Hilger
Date of Publication (YYYY-MM-DD): 2007-05-04
Title of Journal: Human Mutation : Variation, Databases, and Disease
Volume: 28
Issue / Number: 7
Start Page: 674
End Page: 682
Document Type: Article
ID: 334809.0


Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation
Authors: Ullmann, Reinhard; Turner, Gillian; Kirchhoff, Maria; Chen, Wei; Tonge, Bruce; Rosenberg, Carla; Field, Michael; Vianna-Morgante, Angela M.; Christie, Louise; Krepischi-Santos, Ana C.; Banna, Lynn; Brereton, Avril V.; Hill, Alyssa; Bisgaard, Anne-Marie; Müller, Ines; Hultschig, Claus; Erdogan, Fikret; Wieczorek, Georg; Ropers, Hans-Hilger
Date of Publication (YYYY-MM-DD): 2007-05-04
Title of Journal: Human Mutation : Variation, Databases, and Disease
Volume: 28
Issue / Number: 7
Document Type: Article
ID: 335950.0


The DNA sequence of the human X chromosome
Authors: Sudbrak, Ralf; Beck, Alfred; Heitmann, Katja; Hennig, Steffen; Klages, Sven; Kosiura, Anna; Mueller, Ines; Reinhardt, Richard; Lehrach, Hans; et al, ...
Date of Publication (YYYY-MM-DD): 2005-02-01
Title of Journal: Nature
Volume: 343
Issue / Number: 7031
Start Page: 325
End Page: 337
Document Type: Article
ID: 272855.0


The DNA sequence of the human X chromosome
Authors: Sudbrak, Ralf; Beck, Alfred; Heitmann, Katja; Hennig, Steffen; Klages, Sven; Kosiura, Anna; Mueller, Ines; Reinhardt, Richard; Lehrach, Hans; et al
Date of Publication (YYYY-MM-DD): 2005-02-01
Title of Journal: Nature
Volume: 343
Issue / Number: 7031
Start Page: 325
End Page: 337
Document Type: Article
ID: 272857.0


The mouse homeobox gene Not is required for caudal notochord development and affected by the truncate mutation
Authors: Abdelkhalek, Hanaa Ben; Beckers, Anja; Schuster-Gossler, Karin; Pavlova, Maria N.; Burkhardt, Hannelore; Lickert, Heiko; Rossant, Janet; Reinhardt, Richard; Schalkwyk, Leonard C.; Müller, Ines; Herrmann, Bernhard G.; Ceolin, Marcelo; Rivera-Pomar, Rolando; Gossler, Achim
Date of Publication (YYYY-MM-DD): 2004-07-15
Title of Journal: Genes and Development
Volume: 18
Issue / Number: 14
Start Page: 1725
End Page: 1736
Document Type: Article
ID: 228887.0


The mouse homeobox gene Not is required for caudal notochord development and affected by the truncate mutation
Authors: Abdelkhalek, Hanaa Ben; Beckers, Anja; Schuster-Gossler, Karin; Pavlova, Maria N.; Burkhardt, Hannelore; Lickert, Heiko; Rossant, Janet; Reinhardt, Richard; Schalkwyk, Leonard C.; Müller, Ines; Herrmann, Bernhard G.; Ceolin, Marcelo; Rivera-Pomar, Rolando; Gossler, Achim
Date of Publication (YYYY-MM-DD): 2004-07-15
Title of Journal: Genes and Development
Volume: 18
Issue / Number: 14
Start Page: 1725
End Page: 1736
Document Type: Article
ID: 229464.0