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Publications by C Yamanaka
Uniparental and Functional X Disomy in Turner Syndrome Patients With Unexplained Mental Retardation and X Derived Marker Chromosomes.
Journal of Medical Genetics
Genetics
Inertial Confinement Fusion: The Quest for Ignition and Energy Gain Using Indirect Drive
Nuclear Fusion
High Energy Physics
Nuclear
Condensed Matter Physics
Related publications
Supernumerary Marker Chromosomes (SMC) and Uniparental Disomy (UPD): Coincidence or Consequence?
Journal of Medical Genetics
Genetics
Homicide, Fragile X Syndrome, and Mental Retardation
Revista Brasileira de Psiquiatria
Psychiatry
Mental Health
A Newly Defined X Linked Mental Retardation Syndrome Associated With Alpha Thalassaemia.
Journal of Medical Genetics
Genetics
Fragile X Mental Retardation Protein Replacement Restores Hippocampal Synaptic Function in a Mouse Model of Fragile X Syndrome
Gene Therapy
Molecular Medicine
Genetics
Molecular Biology
45,x/47,X,i(X)(q10),i(X)(q10)/46,X,i(X)(q10) Isochromosome Xq in Mosaic Turner Syndrome
International Journal of Human Genetics
Genetics
Death in Adults With Prader-Willi Syndrome May Be Correlated With Maternal Uniparental Disomy
Journal of Medical Genetics
Genetics
Horseshoe Kidney With Growth Retardation: Don’t Forget Turner Syndrome
Turkish Journal of Pediatrics
Child Health
Pediatrics
Perinatology
Synaptic Activity in X-Linked Mental Retardation: A Thorny Issue
Journal of Physiology
Physiology
Sports Science
Paternal Uniparental Disomy of Chromosome 13