Alina T Midro
5PUBLICATIONS
13CO-AUTHORS
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Publications (5)
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|Feb 01, 2021
Phenotypic expansion of the BPTF-related neurodevelopmental disorder with dysmorphic facies and distal limb anomalies.Kevin E Glinton, Anna C E Hurst, Kevin M Bowling
|Jun 04, 2020
Characteristic dental pattern with hypodontia and short roots in Fraser syndrome.Felix Kunz, Hülya Kayserili, Alina Midro
|Jan 31, 2020
Two unrelated families with variable expression of Fraser syndrome due to the same pathogenic variant in the FRAS1 gene.Alina T Midro, Beata Stasiewicz-Jarocka, Jan Borys
|Jan 12, 2019
Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies syndrome due to disruption of BPTF in a 35-year-old man initially diagnosed with Silver-Russell syndrome.Alina T Midro, Niels Tommerup, Jan Borys
|Oct 18, 2018
A 23-year follow-up of a male with Hajdu-Cheney syndrome due to NOTCH2 mutation.Alina T Midro, Beata Stasiewicz-Jarocka, Jan Borys
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Frequent Collaborators
2 joint publications
Martin Zenker
1 joint publications
Hülya Kayserili
1 joint publications
Agnes Bloch-Zupan
1 joint publications
Rafał Płoski
1 joint publications
Kevin E Glinton
1 joint publications
Anna C E Hurst
1 joint publications
Devon Haynes
1 joint publications
Saskia Koene
1 joint publications
Allan Bayat
1 joint publications
Julian Martinez
