Publications by authors named "Florian Marsch"

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Whole exome sequencing identifies a mutation in EYA1 and GLI3 in a patient with branchio‑otic syndrome and esophageal atresia: Coincidence or a digenic mode of inheritance?
Franziska Kause, Heiko Reutter, Florian Marsch, Holger Thiele, Janine Altmüller

Mol Med Rep· February 2018

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Array-based molecular karyotyping in 115 VATER/VACTERL and VATER/VACTERL-like patients identifies disease-causing copy number variations.
Rong Zhang, Florian Marsch, Franziska Kause, Franziska Degenhardt, Eeberhard Schmiedeke

Birth Defects Res· July 2017

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Copy number variations in 375 patients with oesophageal atresia and/or tracheoesophageal fistula.
Erwin Brosens, Florian Marsch, Elisabeth M de Jong, Hitisha P Zaveri, Alina C Hilger

Eur J Hum Genet· December 2016

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Array-based molecular karyotyping in fetuses with isolated brain malformations identifies disease-causing CNVs.
Madita Schumann, Andrea Hofmann, Sophia K Krutzke, Alina C Hilger, Florian Marsch

J Neurodev Disord· April 2016

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CNV analysis in 169 patients with bladder exstrophy-epispadias complex.
Catharina von Lowtzow, Andrea Hofmann, Rong Zhang, Florian Marsch, Anne-Karoline Ebert

BMC Med Genet· April 2016

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