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Author/Creator Hilger, Alina

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 fetal brain malformations: Identification of novel candidate genes and chromosomal regions. Issue 1 (17th December 2015)

Authors:
Krutzke, Sophia K.; Engels, Hartmut; Hofmann, Andrea; Schumann, Madita M.; Cremer, Kirsten; Zink, Alexander M.; Hilger, Alina; Ludwig, Michael; Gembruch, Ulrich; Reutter, Heiko; Merz, Waltraut M.
Journal:
Birth defects research
Issue:
Volume 106:Issue 1(2016)
Page Start:
16
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. De novo 13q deletions in two patients with mild anorectal malformations as part of VATER/VACTERL and VATER/VACTERL‐like association and analysis of EFNB2 in patients with anorectal malformations. Issue 12 (16th August 2013)

Authors:
Dworschak, Gabriel C.; Draaken, Markus; Marcelis, Carlo; de Blaauw, Ivo; Pfundt, Rolph; van Rooij, Iris A.L.M.; Bartels, Enrika; Hilger, Alina; Jenetzky, Ekkehart; Schmiedeke, Eberhard; Grasshoff‐Derr, Sabine; Schmidt, Dominik; Märzheuser, Stefanie; Hosie, Stuart; Weih, Sandra; Holland‐Cunz, Stef...
Journal:
American journal of medical genetics
Issue:
Volume 161:Issue 12(2013:Dec.)
Page Start:
3035
Record Type:
Journal Article
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4. De novo 13q deletions in two patients with mild anorectal malformations as part of VATER/VACTERL and VATER/VACTERL‐like association and analysis of EFNB2 in patients with anorectal malformations. Issue 12 (16th August 2013)

Authors:
Dworschak, Gabriel C.; Draaken, Markus; Marcelis, Carlo; de Blaauw, Ivo; Pfundt, Rolph; van Rooij, Iris A.L.M.; Bartels, Enrika; Hilger, Alina; Jenetzky, Ekkehart; Schmiedeke, Eberhard; Grasshoff‐Derr, Sabine; Schmidt, Dominik; Märzheuser, Stefanie; Hosie, Stuart; Weih, Sandra; Holland‐Cunz, Stef...
Journal:
American journal of medical genetics
Issue:
Volume 161:Issue 12(2013:Dec.)
Page Start:
3035
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

5. Whole exome sequencing and array‐based molecular karyotyping as aids to prenatal diagnosis in fetuses with suspected Simpson–Golabi–Behmel syndrome. (27th September 2016)

Authors:
Kehrer, Christina; Hoischen, Alexander; Menkhaus, Ralf; Schwab, Eva; Müller, Andreas; Kim, Sarah; Kreiß, Martina; Weitensteiner, Valerie; Hilger, Alina; Berg, Christoph; Geipel, Anne; Reutter, Heiko; Gembruch, Ulrich
Journal:
Prenatal diagnosis
Issue:
Volume 36:Number 10(2016)
Page Start:
961
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗