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Alina T Midro

5PUBLICATIONS

13CO-AUTHORS

NeonatologyCraniofacial biologyNon-Newtonian fluid flows (incl. rheology)MechanobiologySocial program evaluation

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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

Frequent Collaborators

2 joint publications

Martin Zenker

1 joint publications

Hülya Kayserili

1 joint publications

Agnes Bloch-Zupan

1 joint publications

Rafał Płoski

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