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Author/Creator Neesen, Juergen

1. High Prevalence of MYO6 Variants in an Austrian Patient Cohort With Autosomal Dominant Hereditary Hearing Loss. Issue 6 (July 2021)

Authors:
Frohne, Alexandra; Koenighofer, Martin; Liu, David Tianxiang; Laccone, Franco; Neesen, Juergen; Gstoettner, Wolfgang; Schoefer, Christian; Lucas, Trevor; Frei, Klemens; Parzefall, Thomas
Journal:
Otology & neurotology
Issue:
Volume 42:Issue 6(2021)
Page Start:
Record Type:
Journal Article
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2. Hydrocephalus, agenesis of the corpus callosum, and cleft lip/palate represent frequent associations in fetuses with Peters' plus syndrome and B3GALTL mutations. – Fetal PPS phenotypes, expanded by Dandy Walker cyst and encephalocele. (13th November 2012)

Authors:
Schoner, Katharina; Kohlhase, Juergen; Müller, Annette M.; Schramm, Thomas; Plassmann, Margit; Schmitz, Ralf; Neesen, Juergen; Wieacker, Peter; Rehder, Helga
Journal:
Prenatal diagnosis
Issue:
Volume 33:Number 1(2013:Jan.)
Page Start:
75
Record Type:
Journal Article
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3. Piepkorn type of osteochondrodysplasia: Defining the severe end of FLNB‐related skeletal disorders in three fetuses and a 106‐year‐old exhibit. Issue 7 (23rd May 2018)

Authors:
Rehder, Helga; Laccone, Franco; Kircher, Susanne G.; Schild, Ralf L.; Rapp, Christiane; Bald, Rainer; Schulze, Bernt; Behunova, Jana; Neesen, Juergen; Schoner, Katharina
Journal:
American journal of medical genetics
Issue:
Volume 176:Issue 7(2018)
Page Start:
1559
Record Type:
Journal Article
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