Zhi-ping J. Tan

Pingshan, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 24 publications

LRRC56 deficiency cause motile ciliopathies in humans and mice.

LRRC56 deficiency cause motile ciliopathies in humans and mice.

Journal: Frontiers in genetics

Published: July 02, 2025

Whole lung lavage in the case of hereditary pulmonary alveolar proteinosis

Whole lung lavage in the case of hereditary pulmonary alveolar proteinosis

Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics

Published: April 07, 2022

CircRNA Microarray Profiling Reveals hsa_circ_0058493 as a Novel Biomarker for Imatinib-Resistant CML.

CircRNA Microarray Profiling Reveals hsa_circ_0058493 as a Novel Biomarker for Imatinib-Resistant CML.

Journal: Frontiers in pharmacology

Published: June 22, 2021

Case Report: BAF-Opathies/SSRIDDs Due to a de novo ACTL6A Variant, Previously Considered to Be Heart-Hand Syndrome.

Case Report: BAF-Opathies/SSRIDDs Due to a de novo ACTL6A Variant, Previously Considered to Be Heart-Hand Syndrome.

Journal: Frontiers in cardiovascular medicine

Published: May 11, 2021

Case Report: Mutant SCN9A Susceptible to Charcot Neuroarthropathy in a Patient With Congenital Insensitivity to Pain.

Case Report: Mutant SCN9A Susceptible to Charcot Neuroarthropathy in a Patient With Congenital Insensitivity to Pain.

Journal: Frontiers in neuroscience

Published: April 19, 2021

A Novel Nonsense MMP21 Variant Causes Dextrocardia and Congenital Heart Disease in a Han Chinese Patient.

A Novel Nonsense MMP21 Variant Causes Dextrocardia and Congenital Heart Disease in a Han Chinese Patient.

Journal: Frontiers in cardiovascular medicine

Published: July 11, 2020

Whole-exome sequencing reveals doubly novel heterozygous Myosin Binding Protein C and Titin mutations in a Chinese patient with severe dilated cardiomyopathy.

Whole-exome sequencing reveals doubly novel heterozygous Myosin Binding Protein C and Titin mutations in a Chinese patient with severe dilated cardiomyopathy.

Journal: Cardiology in the young

Published: August 16, 2018

A Novel Homozygous SACS Mutation Identified by Whole-Exome Sequencing in a Consanguineous Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay.

A Novel Homozygous SACS Mutation Identified by Whole-Exome Sequencing in a Consanguineous Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay.

Journal: Cytogenetic and genome research

Published: April 05, 2017

An effective combination of whole-exome sequencing and runs of homozygosity for the diagnosis of primary ciliary dyskinesia in consanguineous families.

An effective combination of whole-exome sequencing and runs of homozygosity for the diagnosis of primary ciliary dyskinesia in consanguineous families.

Journal: Scientific reports

Published: July 07, 2016

19p13.2 Microdeletion including NFIX associated with overgrowth and intellectual disability suggestive of Malan syndrome.

19p13.2 Microdeletion including NFIX associated with overgrowth and intellectual disability suggestive of Malan syndrome.

Journal: Molecular cytogenetics

Published: February 26, 2016

Identification of two novel mutations in the SLCO2A1 prostaglandin transporter gene in a Chinese patient with primary hypertrophic osteoarthropathy.

Identification of two novel mutations in the SLCO2A1 prostaglandin transporter gene in a Chinese patient with primary hypertrophic osteoarthropathy.

Journal: Molecular medicine reports

Published: January 27, 2016

A clinical and molecular analysis of a patient with Emanuel syndrome.

A clinical and molecular analysis of a patient with Emanuel syndrome.

Journal: Molecular medicine reports

Published: November 21, 2015

Showing 1-12 of 24

Last Updated: 09/26/2026