List of works - Inas S Mostafa - Paulina

List of works by Inas S Mostafa

A homozygous IER3IP1 mutation causes microcephaly with simplified gyral pattern, epilepsy, and permanent neonatal diabetes syndrome (MEDS).

scientific article published on 18 September 2012

KBG syndrome in two patients from Egypt

scientific article published on 28 March 2020

Microcephalic osteodysplastic primordial dwarfism type II: Additional nine patients with implications on phenotype and genotype correlation

scientific article published on 08 April 2020

PUS7 mutations impair pseudouridylation in humans and cause intellectual disability and microcephaly

scientific article published on 18 February 2019

Phenotypic and molecular insights into PQBP1 -related intellectual disability

scientific article published on 23 September 2018

Philtrum length and intercommissural distance measurements at mixed dentition period.

scientific article published in May 2018

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