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Yulia Ariani Aswin
Yulia Ariani Aswin
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Title
Cited by
Cited by
Year
AB016. Developing diagnostic strategy of multiple congenital anomalies in Indonesia
DR Sjarif, YA Aswin
Annals of Translational Medicine 3 (Suppl 2), AB016-AB016, 2015
12015
Molecular analysis in exons 1 and 2 of the tripeptidyl peptidase 1 (TPP1) gene on patients with neuronal ceroid lipofuscinosis type 2 (CLN2) in Indonesia
S Evani, HS Pangestu, MR Arisandi, NM Prakoso, R Priambodo, ...
AIP Conference Proceedings 2710 (1), 2024
2024
Profil Aberasi Kromosom Pasien Malformasi Kongenital Multipel Non-Sindromik
YA Aswin, R Abi Rachmadi
eJournal Kedokteran Indonesia, 114-20, 2022
2022
DATA COLLECTION OF GENE VARIATIONS AND ANALYSIS OF THREE-DIMENSIONAL STRUCTURE OF PROTEINS ASSOCIATED WITH HAIR AGING
AA Putri, NM Prakoso, I Muhiardi, YA Aswin, A Bowolaksono
The 2ndNational Conference for Ummah Network 2021 (INTER-UMMAH 2021) And the …, 2021
2021
THREE-DIMENSIONAL ANALYSIS OF SINGLE NUCLEOTIDE POLYMORPHISMS ASSOCIATED WITH HUMAN SKIN AGING
TSP Adrianto, YA Aswin, NM Prakoso, I Muhiardi, A Bowolaksono
The 2ndNational Conference for Ummah Network 2021 (INTER-UMMAH 2021) And the …, 2021
2021
Variant identification of exon 11 of galactosamine (N-acetyl)-6-sulfatase (GALNS) gene in mucopolysaccharidosis type IVA patients in Indonesia
RAR Sulaiman, RP Aji, NM Prakoso, R Priambodo, YA Aswin, CN Hafifah, ...
AIP Conference Proceedings 2331 (1), 2021
2021
Identification of novel mutations in exon 1 of iduronate-2-sulfatase gene from mucopolysaccharidosis type II patient in Indonesia
AR Widyaningrum, NM Prakoso, R Priambodo, YA Aswin, CN Hafifah, ...
AIP Conference Proceedings 2331 (1), 2021
2021
AB170. Loss of heterozygosity in child with multiple congenital anomaly
YA Aswin, DR Sjarif
Annals of Translational Medicine 3 (Suppl 2), AB170-AB170, 2015
2015
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