Miriam Elbracht (M Elbracht)

Publication Activity (10 Years)

Years Active: 2018-2021
Publications (10 Years): 5

Top Topics

Gold Nanoparticles

Top Venues

Clinical genetics

Molecular genetics & genomic medicine

American journal of medical genetics. Part A

This page only lists publications with an associated author ORCID identifier.

Publications

Miriam Elbracht, Robert Meyer, Kim Kricheldorf, Deniz Gezer, Eggermann Thomas, Beate Betz, Ingo Kurth, Lino L Teichmann, Tim Henrik Brümmendorf, Ulrich Germing, Susanne Isfort, Steffen Koschmieder
Germline variants in DNA repair genes, including BRCA1/2, may cause familial myeloproliferative neoplasms. Blood advances 5 (17) (2021)
Robert Meyer, Miriam Elbracht, Thomas Opladen, Eggermann Thomas
Patient with an autosomal-recessive MBTPS1-linked phenotype and clinical features of Silver-Russell syndrome. American journal of medical genetics. Part A 182 (11) (2020)
Robert Meyer, Matthias Begemann, Stephanie Demuth, Florian Kraft, Daniela Dey, Herdit Schüler, Sabine Busse, Martin G Häusler, Klaus Zerres, Ingo Kurth, Eggermann Thomas, Miriam Elbracht
Inherited cases of CNOT3-associated intellectual developmental disorder with speech delay, autism, and dysmorphic facies. Clinical genetics 98 (4) (2020)
G Gillessen-Kaesbach, B Albrecht, Eggermann Thomas, Miriam Elbracht, D Mitter, S Morlot, C M A van Ravenswaaij-Arts, S Schulz, G Strobl-Wildemann, K Buiting, Jasmin Beygo
Molecular and clinical studies in 8 patients with Temple syndrome. Clinical genetics 93 (6) (2018)
Eggermann Thomas, Susanne Ledig, Matthias Begemann, Miriam Elbracht, Ingo Kurth, Peter Wieacker
Search for altered imprinting marks in Mayer-Rokitansky-Küster-Hauser patients. Molecular genetics & genomic medicine 6 (6) (2018)