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- [31] Xq27.3-q28 Duplication Containing FMR1 Gene: Case Presentation and Literature Review of Familial X-linked Hypogonadism, Gynecomastia, Short Stature, Intellectual Disability and Obesity Syndrome HORMONE RESEARCH IN PAEDIATRICS, 2024, 97 : 376 - 376
- [32] Molecular cytogenetic characterization of a de novo chromosome 1q41-q42.11 microdeletion of paternal origin in a 15-year-old boy with mental retardation, developmental delay, autism and congenital heart defects TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2021, 60 (02): : 341 - 344