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Publications by Duyen Pham
A Non-Coding Variant in the 5ʹ UTR of DLG3 Attenuates Protein Translation to Cause Non-Syndromic Intellectual Disability
European Journal of Human Genetics
Genetics
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Rare Non-Syndromic Intellectual Disability
Subtle Functional Defects in the Arf-Specific Guanine Nucleotide Exchange Factor IQSEC2 Cause Non-Syndromic X-Linked Intellectual Disability
Small GTPases
Biochemistry
Cell Biology
Insight to FBXO31 Novel Mutation p.Cys283Asn Causing Non‑Syndromic Autosomal Recessive Intellectual Disability Using Computational Methods
Clinical Proteomics and Bioinformatics
EstablishingSONin 21q22.11 as a Cause a New Syndromic Form of Intellectual Disability: Possible Contribution to Braddock-Carey Syndrome Phenotype
American Journal of Medical Genetics, Part A
Genetics
Non-Progressive Cerebellar Ataxia With Intellectual Disability
Non-Syndromic Aortic Valve Myxoma in a Teen, Cause of Angina Symptoms
Journal of Cardiothoracic Surgery
Cardiology
Cardiovascular Medicine
Medicine
Pulmonary
Respiratory Medicine
Surgery
Xp11.22 Deletions Encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a Cause of Syndromic X-Linked Intellectual Disability
PLoS ONE
Multidisciplinary
RPGR-containing Protein Complexes in Syndromic and Non-Syndromic Retinal Degeneration Due to Ciliary Dysfunction
Journal of Genetics
Genetics
Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability
American Journal of Human Genetics
Genetics