Rena B. Sihombing
Semarang, JT, Indonesia
Last Updated: 09/26/2026
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Found 9 publications
Phenotypic variability of Fragile-X syndrome in Asian population: A systematic review.
Journal: Intractable & rare diseases research
Published: April 21, 2026
Early identification and treatment of genetic and neurodevelopmental disorders.
Journal: Journal of intellectual disability research : JIDR
Published: July 08, 2024
Genetic diagnostic approach to intellectual disability and multiple congenital anomalies in Indonesia.
Journal: Intractable & rare diseases research
Published: January 09, 2023
Adaptive Stigma Coping Among Papuans Living with HIV: a Qualitative Study in One of the Indigenous People, Indonesia.
Journal: Journal of racial and ethnic health disparities
Published: June 23, 2022
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
Pathogenic variant in NFIX gene affecting three sisters due to paternal mosaicism.
Journal: American journal of medical genetics. Part A
Published: February 06, 2020
Repeat expansion and methylation-sensitive triplet-primed polymerase chain reaction for fragile X mental retardation 1 gene screening in institutionalised intellectually disabled individuals.
Journal: Singapore medical journal
Published: January 29, 2020
Duplication of 1q31.3q41 in two affected siblings due to paternal insertional translocation.
Journal: BMJ case reports
Published: September 02, 2019
Showing 1-9 of 9
Last Updated: 09/26/2026