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Publications by Yihua Ge
Novel Variant in the FGD1 Gene Causing Aarskog-Scott Syndrome
Experimental and Therapeutic Medicine
Medicine
Cancer Research
Immunology
Microbiology
Related publications
Two Novel Mutations Confirm FGD1 Is Responsible for the Aarskog Syndrome
European Journal of Human Genetics
Genetics
A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome
Frontiers in Pediatrics
Child Health
Pediatrics
Perinatology
Novel Mutation in KCNQ2 Causing Ohtahara Syndrome
Annals of Child Neurology
Novel FSHR Variants Causing Female Resistant Ovary Syndrome
Molecular genetics & genomic medicine
Genetics
Molecular Biology
BCS1L Gene Mutation Causing GRACILE Syndrome: Case Report
Renal Failure
Medicine
Nephrology
Critical Care
Intensive Care Medicine
IPEX Syndrome in Siblings With a Novel Variant in FOXP3
Journal of Allergy and Clinical Immunology
Allergy
Immunology
Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient With Androgen Insensitivity Syndrome
Journal of Pediatric and Adolescent Gynecology
Child Health
Gynecology
Perinatology
Obstetrics
Medicine
Pediatrics
Genetic Variant Rs17225178 in the ARNT2 Gene Is Associated With Asperger Syndrome
Molecular Autism
Psychiatry
Mental Health
Developmental Neuroscience
Developmental Biology
Molecular Biology
Long-Term Survival in TARP Syndrome and Confirmation ofRBM10as the Disease-Causing Gene
American Journal of Medical Genetics, Part A
Genetics
