Saeed Farajzadeh Valilou

2PUBLICATIONS
2CO-AUTHORS
Developmental genetics (incl. sex determination)Medical biochemistry - proteins and peptides (incl. medical proteomics)
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Publications (2)

|Feb 09, 2023
Eighth case of Li-Campeau syndrome in a Turkish patient caused by a novel pathogenic variant in UBR7 and expanding the phenotype.

Masoud Edizadeh, Hande Kaymakcalan, Saeed Farajzadeh Valilou

|Sep 01, 2021
A novel biallelic LMNB2 variant in a patient with progressive myoclonus epilepsy and ataxia: A case of laminopathy.

Saeed Farajzadeh Valilou, Javad Karimzad Hagh, Mohammad Salimi Asl

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Frequent Collaborators

1 joint publications

Arash Pooladi

1 joint publications

Hande Kaymakcalan