مرض فقر الدم المنجلي Sickle cell anemia

المؤلف : أ.د. مها علي فهمي صدقي

المصدر : اساسيات علم الوراثة ( الصفات والامراض الوراثية )

الجزء والصفحة : ص170-173

2025-01-22 1967

المزيد

DiGeorge Syndrome

writer : Wass, J. A. H., Arlt, W., & Semple, R. K. (Eds.).

source : Oxford Textbook of Endocrinology and Diabetes

page : 3rd edition , p692

2026-06-28 591

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Types of Gene mutations

writer : Bezabeh ,M. ; Tesfaye,A.; Ergicho, B.; Erke, M.; Mengistu, S. ; Bedane,A. and Desta, A

source : General Pathology

page :

21-2-2016 2897

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The Current State of Treatment of Genetic Disease

writer : Cohn, R. D., Scherer, S. W., & Hamosh, A.

source : Thompson & Thompson Genetics and Genomics in Medicine

page : 9th E, P293-295

2026-01-22 821

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Selenoprotein Deficiency— A Disorder of Thyroid Hormone Metabolism

writer : Wass, J. A. H., Arlt, W., & Semple, R. K. (Eds.).

source : Oxford Textbook of Endocrinology and Diabetes

page : 3rd edition , p566

2026-05-16 785

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Complications of Thalassemia and Their Management: Skeletal Changes

writer : Hoffman, R., Benz, E. J., Silberstein, L. E., Heslop, H., Weitz, J., & Salama, M. E.

source : Hematology : Basic Principles and Practice

page : 8th E , P571-572

2026-04-22 685

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Factors Predisposing to Thyroid cancer

writer : Wass, J. A. H., Arlt, W., & Semple, R. K. (Eds.).

source : Oxford Textbook of Endocrinology and Diabetes

page : 3rd edition , p600-601

2026-05-21 654

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Monogenic Causes of Diabetes : Glucokinase MODY

writer : Holt, Richard IG, and Allan Flyvbjerg

source : Textbook of diabetes (2024)

page : 6th ed , page279-280

2025-12-14 785

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Mechanisms of Disease

writer : Hoffman, R., Benz, E. J., Silberstein, L. E., Heslop, H., Weitz, J., & Salama, M. E.

source : Hematology : Basic Principles and Practice

page : 8th E , P21-22

2025-03-23 1518

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أهم الفحوصات التي تجرى لتشخيص الأمراض الوراثية

المؤلف : ا.د. شيماء جمال احمد , أ.م.د. محمد فاضل إبراهيم

المصدر : كيفية الوقاية من الامراض الوراثية

الجزء والصفحة : ص300-302

2025-01-14 2705

المزيد

Apparent Mineralocorticoid excess

writer : Wass, J. A. H., Arlt, W., & Semple, R. K. (Eds.).

source : Oxford Textbook of Endocrinology and Diabetes

page : 3rd edition , p866-867

2026-07-29 669

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Complete GH Insensitivity (OMIM 262500)

writer : Wass, J. A. H., Arlt, W., & Semple, R. K. (Eds.).

source : Oxford Textbook of Endocrinology and Diabetes

page : 3rd edition , p1118

2026-09-24 405

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Familial Hypercholesterolemia: A Genetic Hyperlipidemia

writer : Cohn, R. D., Scherer, S. W., & Hamosh, A.

source : Thompson & Thompson Genetics and Genomics in Medicine

page : 9th E, P263-267

2026-01-03 984

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سلسلة نقل الإلكترونات Electron Transport Chain

المؤلف : زهرة محمود الخفاجي

المصدر : موسوعة الحياة

الجزء والصفحة :

28-2-2018 2575

المزيد

Deletion and Duplication Syndromes

writer : Cohn, R. D., Scherer, S. W., & Hamosh, A.

source : Thompson & Thompson Genetics and Genomics in Medicine

page : 9th E, P86-88

2025-12-04 1024

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Hemoglobin E: A Structurally Altered Hemoglobin With Thalassemia Phenotypes

writer : Cohn, R. D., Scherer, S. W., & Hamosh, A.

source : Thompson & Thompson Genetics and Genomics in Medicine

page : 9th E, P245

2025-12-25 804

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Steroid Acute Regulatory Protein (stAR) Deficiency— congenital Lipoid Adrenal Hyperplasia

writer : Wass, J. A. H., Arlt, W., & Semple, R. K. (Eds.).

source : Oxford Textbook of Endocrinology and Diabetes

page : 3rd edition , p939

2026-08-18 639

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The Example of Diseases Related to the X Chromosome: Hemophilia A and B

writer : Marcello Ciaccio

source : Clinical and Laboratory Medicine Textbook 2021

page : p569-570

2025-12-30 940

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