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  1. Heterozygous deletion of the VEGFC gene in 4q34.3 is associated with Milroy‐like lymphedema: First prenatal case report

    Article • American Journal of Medical Genetics Part A, September 2022, Wiley

    Dr Minh-Tuan HUYNH

  2. Novel TMEM67 mutations in a Vietnamese family with Joubert syndrome

    Article • BMC Medical Genetics, January 2020, Springer Science + Business Media

    Dr Minh-Tuan HUYNH

  3. Clinical characteristics and genetic profiles of young and adult patients with cholestatic liver disease

    Article • Revista Española de Enfermedades Digestivas, January 2019, Sociedad Espanola de Patologia Digestiva (SEPD)

    Dr Minh-Tuan HUYNH

  4. Novel compound heterozygous ABCC2 variants in patients with Dubin-Johnson syndrome and intrahepatic cholestasis of pregnancy

    Article • August 2018, Wiley

    Dr Minh-Tuan HUYNH, Cong Toai Tran, Minh Tuan HUYNH

  5. 15q24.1 BP4-BP1 microdeletion unmasking paternally inherited functional polymorphisms combined with distal 15q24.2q24.3 duplication in a patient with epilepsy, psychomotor delay, overweight, ventricular arrhythmia

    Article • European Journal of Medical Genetics, August 2018, Elsevier

    Dr Minh-Tuan HUYNH

  6. A heterozygous microdeletion of 20q13.13 encompassing ADNP gene in a child with Helsmoortel–van der Aa syndrome

    Article • European Journal of Human Genetics, June 2018, Springer Science + Business Media

    Dr Minh-Tuan HUYNH

  7. First prenatal case of proximal 19p13.12 microdeletion syndrome: New insights and new delineation of the syndrome

    Article • European Journal of Medical Genetics, June 2018, Elsevier

    Dr Minh-Tuan HUYNH

  8. ABCB4 sequence variants in adult cholestatic liver diseases

    Article • Revista Española de Enfermedades Digestivas, January 2018, Sociedad Espanola de Patologia Digestiva (SEPD)

    Dr Minh-Tuan HUYNH

  9. WAGR syndrome and congenital hypothyroidism in a child with a Mosaic 11p13 deletion

    Article • American Journal of Medical Genetics Part A, April 2017, Wiley

    Minh Tuan HUYNH, Cong Toai Tran, Dr Minh-Tuan HUYNH

  10. RUNX1T1, a chromatin repression protein, is a candidate gene for autosomal dominant intellectual disability

    Article • American Journal of Medical Genetics Part A, May 2012, Wiley

    Dr Minh-Tuan HUYNH

  11. Culture and differentiation of osteoblasts on coral scaffold from human bone marrow mesenchymal stem cells

    Article • Cell and Tissue Banking, August 2010, Springer Science + Business Media

    Dr Minh-Tuan HUYNH

  12. In vitro culture of Keratinocytes from human umbilical cord blood mesenchymal stem cells: the Saigonese culture

    Article • Cell and Tissue Banking, March 2010, Springer Science + Business Media

    Dr Minh-Tuan HUYNH

  13. Report Case: Cultured Keratinocyte Autograft on Collagen from Amniotic Membrane for Treatment the Injured Human Skin

    Article • January 2010, Springer Science + Business Media

    Dr Minh-Tuan HUYNH