Zehra Agha

4PUBLICATIONS
2CO-AUTHORS
NeurogeneticsGenetics not elsewhere classifiedCell and nuclear division
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Publications (4)

|Jan 08, 2025
Denovo variants in POGZ and YY1 genes: The novel mega players for neurodevelopmental syndromes in two unrelated consanguineous families.

Behjat Ul Mudassir, Mujaddid Mudassir, Jamal B Williams

|Jan 08, 2025
Genetic Heterogeneity in Four Probands Reveals HGSNAT, KDM6B, LMNA and WFS1 Related Neurodevelopmental Disorders.

Behjat Ul Mudassir, Mujaddid Mudassir, Jamal B Williams

|Jun 28, 2023
Novel biallelic frameshift in TRPM7 gene causes Hallermann-Streiff syndrome in a consanguineous family: a case report.

Behjat Ul Mudassir, Zehra Agha

|Jun 28, 2023
Microcephaly, Short Stature, Intellectual Disability, Speech Absence and Cataract Are Associated with Novel Bi-Allelic Missense Variant in RTTN Gene: A Seckel Syndrome Case Report.

Behjat Ul Mudassir, Zehra Agha

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Frequent Collaborators

3 joint publications

Behjat Ul Mudassir

1 joint publications

Jamal B Williams