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Birgitta Gläser

*born* 1968

*BiographicalDetails*
Diss. Fakultät für Biologie

*Variants*
Birgitta Christiane Gläser

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1

Marfan syndrome caused by disruption of the FBN1 gene due to a reciprocal chromosome translocation

Schnause, Anna Clara (Verfasser)

Freiburg : Universität, 2021

*eBook*

2

Obsessive-compulsive symptoms and heterozygous microduplication of the RB1CC1 gene

Maier, Alexander (Verfasser)

Freiburg : Universität, 2025

*eBook*

3

CRISPR-Cas12a for highly efficient and marker-free targeted integration in human pluripotent stem cells

Hammad, Ruba (Verfasser)

Freiburg : Universität, 2024

*eBook*

4

Heterozygous deletion of SCN2A and SCN3A in a patient with autism spectrum disorder and Tourette syndrome: a case report

Nickel, Kathrin Alexandra (Verfasser)

Freiburg : Universität, 2018

*eBook*

5

New Cav1.2 channelopathy with high-functioning autism, affective disorder, severe dental enamel defects, a short QT interval, and a novel CACNA1C loss-of-function mutation

Endres, Dominique (Verfasser)

Freiburg : Universität, 2020

*eBook*

6

Schizophrenia and hereditary polyneuropathy : : PMP22 deletion as a common pathophysiological link?

Endres, Dominique (Verfasser)

Freiburg : Universität, 2019

*eBook*

7

Modeling MyD88 deficiency In vitro provides new insights in its function

Craig-Müller, Nils (Verfasser)

Freiburg : Universität, 2021

*eBook*