Inherited deletion of 1q, hyperparathyroidism and signs of y-chromosomal influence in a patient with turner syndrome

Keyphrases

• Aortic Coarctation 16%
• Atypical Features 16%
• Behavior Problems 33%
• Behavioral Evidence 16%
• Blood Samples 16%
• CDC73 16%
• Chromosomal Microarray 33%
• Clinical Characteristics 16%
• Copy number Variation 16%
• Cytogenetic Characterization 16%
• Diagnostic Modalities 16%
• Fluorescence in Situ Hybridization 33%
• Genetic Diagnostics 16%
• Genetic Testing 16%
• Gonadal Dysgenesis 16%
• Gonadal Tissue 16%
• Growth Hormone 16%
• Height Curve 16%
• High Arched Palate 16%
• Hyperparathyroidism 100%
• Hyperparathyroidism-jaw Tumor Syndrome (HPT-JT) 16%
• Inherited Deletion 100%
• Leydig Cells 16%
• Minimal Treatment 16%
• Molecular Characterization 16%
• Molecular Etiology 16%
• Nodule 16%
• Parathyroid Adenoma 50%
• Phenotypic Characterization 16%
• Robust Growth 16%
• Seminiferous Tubules 16%
• Sertoli Cells 16%
• Tissue Sampling 16%
• Turner Syndrome 100%
• Webbed Neck 16%
• X-monosomy 16%
• Y Chromosome 16%

Medicine and Dentistry

• Array Comparative Genomic Hybridization 33%
• Behavioral Issue 16%
• Cancer Syndrome 16%
• Coarctation of the Aorta 16%
• Diagnosis 16%
• Differential Diagnosis 16%
• Fluorescence in Situ Hybridization 33%
• Genetic Screening 16%
• Gonadal Dysgenesis 16%
• Growth Hormone 16%
• High Arched Palate 16%
• Hyperparathyroidism 100%
• Jaw Tumor 16%
• Leydig Cell 16%
• Molecular Pathology 16%
• Monosomy X 16%
• Parathyroid Adenoma 50%
• Problem Behavior 16%
• Seminiferous Tubule 16%
• Sertoli Cell 16%
• Turner Syndrome 100%
• Webbed Neck 16%
• Y Chromosome 16%

Biochemistry, Genetics and Molecular Biology

• Array Comparative Genomic Hybridization 33%
• Bovine Somatotropin 16%
• CDC73 16%
• Cytogenetics 16%
• Fluorescence in Situ Hybridization 33%
• Genetic Screening 16%
• Genetics 16%
• Growth Hormone 16%
• Monosomy 16%
• Problem Behavior 16%
• Seminiferous Tubule 16%
• Sertoli Cell 16%
• Turner Syndrome 100%
• Y Chromosome 16%