Saemah N. Zafar

Rawalpindi, PB, Pakistan

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 26 publications

Prevalence of virulent Candida spp. in complicated urinary tract infection of nephrolithiatic patients from surgical units of tertiary care hospitals Islamabad.

Prevalence of virulent Candida spp. in complicated urinary tract infection of nephrolithiatic patients from surgical units of tertiary care hospitals Islamabad.

Journal: Journal de mycologie medicale

Published: April 02, 2019

Identification of a Novel ZNF469 Mutation in a Pakistani Family With Brittle Cornea Syndrome.

Identification of a Novel ZNF469 Mutation in a Pakistani Family With Brittle Cornea Syndrome.

Journal: Cornea

Published: March 14, 2019

Correction: Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice.

Correction: Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice.

Journal: PLoS genetics

Published: December 27, 2018

Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3' splice acceptor site of intron 2.

Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3' splice acceptor site of intron 2.

Journal: Congenital anomalies

Published: April 27, 2018

Delineation of Novel Autosomal Recessive Mutation in GJA3 and Autosomal Dominant Mutations in GJA8 in Pakistani Congenital Cataract Families.

Delineation of Novel Autosomal Recessive Mutation in GJA3 and Autosomal Dominant Mutations in GJA8 in Pakistani Congenital Cataract Families.

Journal: Genes

Published: January 19, 2018

Variants in the PRPF8 Gene are Associated with Glaucoma.

Variants in the PRPF8 Gene are Associated with Glaucoma.

Journal: Molecular neurobiology

Published: March 29, 2017

Gene mapping in an anophthalmic pedigree of a consanguineous Pakistani family opened new horizons for research.

Gene mapping in an anophthalmic pedigree of a consanguineous Pakistani family opened new horizons for research.

Journal: Balkan journal of medical genetics : BJMG

Published: October 28, 2016

A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma.

A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma.

Journal: PloS one

Published: May 04, 2016

Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma.

Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma.

Journal: PloS one

Published: December 18, 2015

Tumor Regression Patterns in Retinoblastoma.

Tumor Regression Patterns in Retinoblastoma.

Journal: Journal of the College of Physicians and Surgeons--Pakistan : JCPSP

Published: November 18, 2015

Congenital Cataract, Nasolacrimal Duct Obstruction, and Methicillin-Resistant Staphylococcus aureus Conjunctivitis: When to Operate?

Congenital Cataract, Nasolacrimal Duct Obstruction, and Methicillin-Resistant Staphylococcus aureus Conjunctivitis: When to Operate?

Journal: Journal of pediatric ophthalmology and strabismus

Published: October 20, 2015

Anisometropia and Ptosis in Patients with Monocular Elevation Deficiency.

Anisometropia and Ptosis in Patients with Monocular Elevation Deficiency.

Journal: Journal of the College of Physicians and Surgeons--Pakistan : JCPSP

Published: October 19, 2015

Showing 1-12 of 26

Last Updated: 09/26/2026