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Author/Creator Marsch, Florian

1. Array-based molecular karyotyping in fetuses with isolated brain malformations identifies disease-causing CNVs. Issue 1 (December 2016)

Authors:
Schumann, Madita; Hofmann, Andrea; Krutzke, Sophia; Hilger, Alina; Marsch, Florian; Stienen, Dietlinde; Gembruch, Ulrich; Ludwig, Michael; Merz, Waltraut; Reutter, Heiko
Journal:
Journal of neurodevelopmental disorders
Issue:
Volume 8:Issue 1(2016)
Page Start:
1
Record Type:
Journal Article
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2. Array‐based molecular karyotyping in 115 VATER/VACTERL and VATER/VACTERL‐like patients identifies disease‐causing copy number variations. Issue 13 (12th June 2017)

Authors:
Zhang, Rong; Marsch, Florian; Kause, Franziska; Degenhardt, Franziska; Schmiedeke, Eeberhard; Märzheuser, Stefanie; Hoppe, Bernd; Bachour, Haitham; Boemers, Thomas M.; Schäfer, Matthias; Spychalski, Nicole; Neser, Jörg; Leonhardt, Johannes; Kosch, Ferdinand; Ure, Benno; Gómez, Barbara; Lacher, Ma...
Journal:
Birth defects research
Issue:
Volume 109:Issue 13(2017)
Page Start:
1063
Record Type:
Journal Article
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3. CNV analysis in 169 patients with bladder exstrophy-epispadias complex. Issue 1 (December 2016)

Authors:
von Lowtzow, Catharina; Hofmann, Andrea; Zhang, Rong; Marsch, Florian; Ebert, Anne-Karoline; Rösch, Wolfgang; Stein, Raimund; Boemers, Thomas; Hirsch, Karin; Marcelis, Carlo; Feitz, Wouter; Brusco, Alfredo; Migone, Nicola; Di Grazia, Massimo; Moebus, Susanne; Nöthen, Markus; Reutter, Heiko; Ludwi...
Journal:
BMC medical genetics
Issue:
Volume 17:Issue 1(2016)
Page Start:
1
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗