3β- Hydroxysteroid Dehydrogenase type 2 (HSD3B2) Deficiency

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

source : Oxford Textbook of Endocrinology and Diabetes

page : 3rd edition , p938

2026-08-18 29

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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

2026-05-16 500

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Complications of Thalassemia and Their Management: Endocrinopathies

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 , P572

2026-04-22 384

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Polyglutamine Disorders

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

source : Thompson & Thompson Genetics and Genomics in Medicine

page : 9th E, P127-128

2025-12-17 640

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مساعدات الهضم Digestive Aids

المؤلف : زهرة محمود الخفاجي

المصدر : موسوعة الحياة

الجزء والصفحة :

28-1-2018 1151

المزيد

Transient neonatal diabetes

writer : Holt, Richard IG, and Allan Flyvbjerg

source : Textbook of diabetes (2024)

page : 6th ed , page 285

2025-12-21 630

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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

2025-12-04 790

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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 1251

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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

2025-12-25 671

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Clinical and Laboratory Features of Familial Hypocalciuric Hypercalcaemia (FHH)

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

source : Oxford Textbook of Endocrinology and Diabetes

page : 3rd edition , p674-676

2026-06-22 321

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Acute Intermittent Porphyria

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 , P512-513

2026-03-31 443

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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 2280

المزيد

Special Considerations in Treating Genetic Disease

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

source : Thompson & Thompson Genetics and Genomics in Medicine

page : 9th E, P295-296

2026-01-27 476

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Porphyrias: Biologic and Molecular Aspects

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 , P509-511

2026-03-31 416

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Glucose-6-Phosphate Dehydrogenase Deficiency and Rasburicase

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 , P88-89

2025-08-10 1006

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مرض ويلسون Wilsons disease

المؤلف : أ.د. مها علي فهمي صدقي

المصدر : اساسيات علم الوراثة ( الصفات والامراض الوراثية )

الجزء والصفحة : ص182-184

2025-01-27 1484

المزيد

Monogenic Causes of Diabetes : Glucokinase MODY

writer : Holt, Richard IG, and Allan Flyvbjerg

source : Textbook of diabetes (2024)

page : 6th ed , page279-280

2025-12-14 616

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Hypertension Due to congenital Adrenal Hyperplasia

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

source : Oxford Textbook of Endocrinology and Diabetes

page : 3rd edition , p866

2026-07-29 198

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