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Publications by Cheng Ming
A Novel Dominant Mutation in the SOX10 Gene in a Chinese Family With Waardenburg Syndrome Type�II
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
Related publications
Biallelic Deletions of the Waardenburg II Syndrome Gene, SOX10 , Cause a Recognizable Arthrogryposis Syndrome
American Journal of Medical Genetics, Part A
Genetics
a Novel HSF4 Gene Mutation Causes Autosomal-Dominant Cataracts in a Chinese Family
G3: Genes, Genomes, Genetics
Medicine
Genetics
Molecular Biology
Identification of a Novel Frameshift Mutation in PITX2 Gene in a Chinese Family With Axenfeld-Rieger Syndrome
Journal of Zhejiang University: Science B
Genetics
Pharmacology
Molecular Biology
Biochemistry
Veterinary
Medicine
Toxicology
Pharmaceutics
Whole-Exome Sequencing Analysis of Waardenburg Syndrome in a Chinese Family
Human Genome Variation
Biochemistry
Genetics
Molecular Biology
Identification of a Novel TCOF1 Mutation in a Chinese Family With Treacher Collins Syndrome
Experimental and Therapeutic Medicine
Medicine
Cancer Research
Immunology
Microbiology
A Novel P20R Mutation in the Alpha-B Crystallin Gene Causes Autosomal Dominant Congenital Posterior Polar Cataracts in a Chinese Family
BMC Ophthalmology
Medicine
Ophthalmology
A Case of Autosomal Dominant Osteopetrosis Type II With a CLCN7 Gene Mutation
JCRPE Journal of Clinical Research in Pediatric Endocrinology
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
A Novel MIP Gene Mutation Analysis in a Chinese Family Affected With Congenital Progressive Punctate Cataract
PLoS ONE
Multidisciplinary
A Novel Mutation of GARS in a Chinese Family With Distal Hereditary Motor Neuropathy Type V
Frontiers in Neurology
Neurology
