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Marion Döbler-Neumann
Marion Döbler-Neumann
University of Tübingen
Genetics
Biology
Mutation
Pathology
Dominance (genetics)
4
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60
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Pontocerebellar hypoplasia type 11: Does the genetic defect determine timing of cerebellar pathology?
2020
European Journal of Medical Genetics
Lucia Laugwitz
Rebecca Buchert
Samuel Groeschel
Angelika Riess
Mona Grimmel
Stefanie Beck-Wödl
Marc Sturm
Georg Gohla
Marion Döbler-Neumann
Ingeborg Krägeloh-Mann
Tobias B. Haack
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Uniparental disomy of chromosome 16 unmasks recessive mutations of FA2H/SPG35 in 4 families
2016
Neurology
Anne S. Soehn
Tim W. Rattay
Stefanie Beck-Wödl
Karin Schäferhoff
David Monk
Marion Döbler-Neumann
Konstanze Hörtnagel
Agatha Schlüter
Montserrat Ruiz
Aurora Pujol
Stephan L Zuchner
Olaf Riess
Rebecca Schüle
Peter Bauer
Ludger Schöls
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PIK3R1 mutations in SHORT syndrome
2014
Clinical Genetics
Christopher Schroeder
Angelika Riess
Michael Bonin
Peter Bauer
Olaf Riess
Marion Döbler-Neumann
S. Wieser
Ute Moog
Andreas Tzschach
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Citations (26)
Congenital disorder of glycosylation type Ia: benign clinical course in a new genetic variant
2002
Childs Nervous System
Irina Mader
Marion Döbler-Neumann
Wilhelm Küker
Helena Stibler
Ingeborg Krägeloh-Mann
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Citations (17)
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