العربية al-ʿarabīyah Oman: Translations Library
Information for Patients and Families
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العربية عمان al-ʿarabīyah Oman: EuroGenTest Documents
| Web Pages | Documents | |
| ختبار صحة الجنين (Amniocentesis Test) | ||
| التغير في الكروموسومات (Chromosome changes) | ||
| التغير الإنتقالي للكروموسومات (Chromosome translocations) | ||
| اختبار تحليل عينات الزوائد المشيمية (Chorionic Villus Sampling: CVS) | ||
| الوراثة السائدة (Dominant inheritance) | ||
| التشخيص للسرطان طان الوراثي (Inherited cancer) | ||
| ما المقصود بالتشخيص الجيني التنبؤي؟ (Predictive test) | ||
| الوراثة المتنحية (Recessive inheritance) | ||
| ماذا يحدث في مختبر الجينات؟ (What happens in a genetics lab?) | ||
| ما هو الفحص الجيني؟ (What is a genetic test?) | ||
| الوراثة المرتبطة بكروموسوم X (X linked inheritance) |
العربية al-ʿarabīyah: Other Documents
| Web Pages | Documents | |
| 1. General use: | ||
| Interpreter Glossary | ||
| Clinic Information Glossary | ||
| 2. Generic inheritance: | ||
| Autosomal dominant inheritance (diagram showing affected father) |
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| Autosomal dominant inheritance (diagram showing affected mother) |
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| Autosomal recessive inheritance | ||
| X linked inheritance | ||
| Marrying a relative | ||
| 3. Procedures and explanations: | ||
| Pre implantation Genetic diagnosis | ||
| Prenatal diagnosis | ||
| Instructions for providing a mouthwash sample for DNA. | ||
| 4. Generic Chromosomal conditions: | ||
| Translocations | ||
| Robertsonian translocations | ||
| 5. Specific Conditions: | ||
| Cystic Fibrosis | ||
| Di George Syndrome | ||
| Fragile X Syndrome | ||
| Huntington's Disease | ||
| Klinefelter Syndrome | ||
| Marfan Syndrome | ||
| Myotonic dystrophy | ||
| Neurofibromatosis type 1 | ||
| Turner Syndrome | ||
| Triple X Syndrome | ||
| XYY syndrome | ||
| Familial hypercholesterolaemia | ||
| genetic deafness | ||
| 6. Cancer genetics: | ||
| Bowel Cancer | ||
| Breast Cancer | ||
| Hereditary non polyposis colon cancer |