Dr Minh-Tuan HUYNH

  • Universite de Nantes
  • Government Employee, Health Sciences
  • France

My co-authors include

Minh Tuan HUYNH
Cong Toai Tran

Find me at

My Publications

Novel TMEM67 mutations in a Vietnamese family with Joubert syndrome

  • BMC Medical Genetics
  • January 2020

Clinical characteristics and genetic profiles of young and adult patients with cholesta...

  • Revista Española de Enfermedades Digestivas
  • January 2019

Novel compound heterozygous ABCC2 variants in patients with Dubin-Johnson syndrome and...

  • August 2018

15q24.1 BP4-BP1 microdeletion unmasking paternally inherited functional polymorphisms c...

  • European Journal of Medical Genetics
  • August 2018

A heterozygous microdeletion of 20q13.13 encompassing ADNP gene in a child with Helsmoo...

  • European Journal of Human Genetics
  • June 2018

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

  • European Journal of Medical Genetics
  • June 2018

ABCB4 sequence variants in adult cholestatic liver diseases

  • Revista Española de Enfermedades Digestivas
  • January 2018

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

  • American Journal of Medical Genetics Part A
  • April 2017

RUNX1T1, a chromatin repression protein, is a candidate gene for autosomal dominant int...

  • American Journal of Medical Genetics Part A
  • May 2012

Culture and differentiation of osteoblasts on coral scaffold from human bone marrow mes...

  • Cell and Tissue Banking
  • August 2010

In vitro culture of Keratinocytes from human umbilical cord blood mesenchymal stem cell...

  • Cell and Tissue Banking
  • March 2010

Report Case: Cultured Keratinocyte Autograft on Collagen from Amniotic Membrane for Tre...

  • January 2010