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Publications by Ming-Ji Fann
Mouse Model of Congenital Heart Defects, Dysmorphic Facial Features and Intellectual Developmental Disorders as a Result of Non-Functional CDK13
Frontiers in Cell and Developmental Biology
Developmental Biology
Cell Biology
Regulation of Sodium-Calcium Exchanger Activity by Creatine Kinase Under Energy-Compromised Conditions
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
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A Review of the Genomic Analysis of Children Presenting With Developmental Delay/Intellectual Disability and Associated Dysmorphic Features
Cureus
De novoPHIPpredicted Deleterious Variants Are Associated With Developmental Delay, Intellectual Disability, Obesity, and Dysmorphic Features
Cold Spring Harbor molecular case studies
Biochemistry
Molecular Medicine
Genetics
Heterozygous Loss-Of-Function Variants of MEIS2 Cause a Triad of Palatal Defects, Congenital Heart Defects, and Intellectual Disability
European Journal of Human Genetics
Genetics
A New Syndrome of Congenital Hypoparathyroidism, Severe Growth Failure, and Dysmorphic Features.
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Dosage Changes of MED13L Further Delineate Its Role in Congenital Heart Defects and Intellectual Disability
European Journal of Human Genetics
Genetics
Vulnerability of the Developing Heart to Oxygen Deprivation as a Cause of Congenital Heart Defects
Journal of the American Heart Association
Cardiovascular Medicine
Cardiology
Intellectual Disability and Dysmorphic Features in Male Siblings Arising From a Novel TAF1 Mutation
Congenital Anomalies
Child Health
Pediatrics
Perinatology
Medicine
Developmental Biology
Embryology
Neural and Synaptic Defects in Slytherin, a Zebrafish Model for Human Congenital Disorders of Glycosylation
PLoS ONE
Multidisciplinary
Mutations in TKT Are the Cause of a Syndrome Including Short Stature, Developmental Delay, and Congenital Heart Defects
American Journal of Human Genetics
Genetics