Shaheen Shahzad
3PUBLICATIONS
2CO-AUTHORS
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Publications (3)
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|May 26, 2021
An intrafamilial phenotypic variability in Ellis-Van Creveld syndrome due to a novel 27 bps deletion mutation.Ayesha Zaka, Shaheen Shahzad, Hadi Zahid Rao
|Nov 03, 2020
A novel homozygous frameshift mutation in the DCC gene in a Pakistani family with autosomal recessive horizontal gaze palsy with progressive scoliosis-2 with impaired intellectual development.Ayesha Zaka, Shaheen Shahzad, Hadi Zahid Rao
|Sep 16, 2017
Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities.Madiha Rasheed, Shaheen Shahzad, Afifa Zaeem
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