Sultana H. Faradz - Publications

WT1 Deletion in 46,XY DSD: The Importance of Copy Number Variant Analysis.

Journal: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation

Published: September 20, 2025

Detection of FMR1 CGG Repeat Expansions Using Buccal Swab and Blood Samples of Children With Intellectual Disability in A Resource-Limited Country.

Journal: Journal, genetic engineering & biotechnology

Published: March 28, 2025

46,XX males with congenital adrenal hyperplasia: a clinical and biochemical description.

Journal: Frontiers in endocrinology

Published: March 31, 2024

Analysis of Consanguinity as Risk Factor of Nonsyndromic Cleft Lips with or without Palate.

Journal: European journal of dentistry

Published: November 23, 2023

Corrigendum: Challenges in the treatment of late-identified untreated congenital adrenal hyperplasia due to CYP11B1 deficiency: Lessons from a developing country.

Journal: Frontiers in endocrinology

Published: April 23, 2023

Pituitary Macroadenoma in a Girl with Male Karyotype: A Rare Case Study.

Journal: Acta medica Indonesiana

Published: March 31, 2023

Challenges in the treatment of late-identified untreated congenital adrenal hyperplasia due to CYP11B1 deficiency: Lessons from a developing country.

Journal: Frontiers in endocrinology

Published: August 10, 2022

Lessons Learned from 17 Years of Multidisciplinary Care for Differences of Sex Development Patients at a Single Indonesian Center.

Journal: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation

Published: August 07, 2022

Measuring steroids in hair opens up possibilities to identify congenital adrenal hyperplasia in developing countries.

Journal: Clinical endocrinology

Published: January 24, 2022

Differences in thrombin and plasmin generation potential between East African and Western European adults: The role of genetic and non-genetic factors.

Journal: Journal of thrombosis and haemostasis : JTH

Published: September 12, 2021

Clinical lesson learned from genetic analysis in patients prior to surgical repair of hypospadias.

Journal: Asian journal of urology

Published: June 26, 2021

Pathogenic variant in NFIX gene affecting three sisters due to paternal mosaicism.

Journal: American journal of medical genetics. Part A

Published: February 06, 2020