The genetic basis of female reproductive disorders: Etiology and clinical testing

Keyphrases

• Clinical Testing 100%
• Etiology 100%
• Hypogonadotropic Hypogonadism 100%
• Genetic Basis 100%
• Female Reproductive Disorders 100%
• Polycystic Ovary Syndrome 66%
• Leiomyoma 66%
• Endometriosis 66%
• Hypergonadotropic Hypogonadism 66%
• Spontaneous Ovarian Hyperstimulation Syndrome 66%
• Eugonadal 66%
• Fibroblast Growth Factor Receptor 1 (FGFR1) 33%
• Chromosomal Region 33%
• Molecular Biology Techniques 33%
• Genetic Testing 33%
• Kallmann Syndrome 33%
• CHD7 33%
• Gene mutation 33%
• Gonadal Failure 33%
• Germline Gene 33%
• Reproductive Disorders 33%
• Wnt4 33%
• Müllerian Aplasia 33%
• Six Genes 33%
• FSHR mutation 33%
• PROP1 Gene 33%
• Affected Females 33%
• Pituitary Hormone Deficiency 33%
• Fragile X Mental Retardation 1 (FMR1) 33%

Medicine and Dentistry

• Disease 100%
• Hypogonadotropic Hypogonadism 75%
• Angioleiomyoma 50%
• Endometriosis 50%
• Polycystic Ovary Syndrome 50%
• Hypergonadotropic Hypogonadism 50%
• Ovarian Hyperstimulation Syndrome 50%
• Clinician 25%
• Gene Mutation 25%
• Fibroblast Growth Factor Receptor 1 25%
• Genetic Screening 25%
• Kallmann Syndrome 25%
• CHD7 25%
• Hypogonadism 25%
• Aplasia 25%
• Hormone Deficiency 25%
• Hypophysis Hormone 25%
• FMR1 25%