Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Sophia K. Krutzke"'
Autor:
Heiko Reutter, Waltraut M. Merz, Alina C. Hilger, Michael Ludwig, Kirsten Cremer, Sophia K. Krutzke, Hartmut Engels, Ulrich Gembruch, Madita M. Schumann, Andrea Hofmann, Alexander M. Zink
Publikováno v:
Birth Defects Research Part A: Clinical and Molecular Teratology. 106:16-26
BACKGROUND For the majority of congenital brain malformations, the underlying cause remains unknown. Recent studies have implicated rare copy number variations (CNVs) in their etiology. METHODS Here, we used array-based molecular karyotyping to searc
Autor:
Waltraut M. Merz, Andrea Hofmann, Alina C. Hilger, Florian Marsch, Michael Ludwig, Sophia K. Krutzke, Dietlinde Stienen, Heiko Reutter, Madita M. Schumann, Ulrich Gembruch
Publikováno v:
Journal of Neurodevelopmental Disorders
Background The overall birth prevalence for congenital malformations of the central nervous system (CNS) among Europeans may be as high as 1 in 100 live births. The etiological factors remain largely unknown. The aim of this study was to detect causa
Autor:
Sophia K, Krutzke, Hartmut, Engels, Andrea, Hofmann, Madita M, Schumann, Kirsten, Cremer, Alexander M, Zink, Alina, Hilger, Michael, Ludwig, Ulrich, Gembruch, Heiko, Reutter, Waltraut M, Merz
Publikováno v:
Birth defects research. Part A, Clinical and molecular teratology. 106(1)
For the majority of congenital brain malformations, the underlying cause remains unknown. Recent studies have implicated rare copy number variations (CNVs) in their etiology.Here, we used array-based molecular karyotyping to search for causative CNVs