Sultana M. Faradz
Semarang, JT, Indonesia
Last Updated: 09/26/2026
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Found 11 publications
Genetic diagnostic approach to intellectual disability and multiple congenital anomalies in Indonesia.
Journal: Intractable & rare diseases research
Published: January 09, 2023
The aberrant behavior profile in Indonesian individuals with fragile X syndrome with limited genetic services.
Journal: Intractable & rare diseases research
Published: July 11, 2022
Epidermolysis Bullosa and Rickets in a 21-Year-Old Female: A Case Report.
Journal: Case reports in dermatology
Published: January 17, 2022
Meiotic genes in premature ovarian insufficiency: variants in HROB and REC8 as likely genetic causes.
Journal: European journal of human genetics : EJHG
Published: June 29, 2021
Clinical manifestation and genetic analysis of familial rare disease genodermatosis xeroderma pigmentosum.
Journal: Intractable & rare diseases research
Published: May 17, 2021
Surveillance and prevalence of fragile X syndrome in Indonesia.
Journal: Intractable & rare diseases research
Published: February 22, 2021
Duplication of 1q31.3q41 in two affected siblings due to paternal insertional translocation.
Journal: BMJ case reports
Published: September 02, 2019
Genetic Analysis Reveals Complete Androgen Insensitivity Syndrome in Female Children Surgically Treated for Inguinal Hernia.
Journal: Journal of investigative surgery : the official journal of the Academy of Surgical Research
Published: April 24, 2019
The first family with adult osteogenesis imperfecta caused by a novel homozygous mutation in CREB3L1.
Journal: Molecular genetics & genomic medicine
Published: April 09, 2019
Phenotypic Variation of 46,XX Late Identified Congenital Adrenal Hyperplasia among Indonesians.
Journal: Journal of the ASEAN Federation of Endocrine Societies
Published: October 24, 2017
Distribution of AGG interruption patterns within nine world populations.
Journal: Intractable & rare diseases research
Published: October 31, 2014
Showing 1-11 of 11
Last Updated: 09/26/2026