Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics
portes grátis
Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics
Hematologic, Renal, and Immunologic Disorders
Korf, Bruce R.; Pyeritz, Reed E.; Grody, Wayne W.
Elsevier Science Publishing Co Inc
08/2022
382
Dura
Inglês
9780128125342
15 a 20 dias
450
Descrição não disponível.
Section 1 1. Hemoglobinopathies and Thalassemias 2. Other Hereditary Red Blood Cell Disorders 3. Hemophilias and Other Disorders of Hemostasis 4. Rhesus and Other Fetomaternal Incompatibilities
Section 2 5. Systemic Lupus Erythematosus 6. Rheumatoid Disease and Other Inflammatory Arthropathies 7. Amyloidosis and Other Protein Deposition Diseases 8. Immunodeficiency Disorders 9. Inherited Complement Deficiencies 10. Inflammatory Disorders 11. Celiac Disease 12. Disorders of Leukocyte Function
Section 3 13. Genetic Disorders of the Pituitary Gland 14. Thyroid Disorders 15. Parathyroid Disorders, 16. Diabetes Mellitus 17. Genetic Disorders of the Adrenal Gland 18. Disorders of the Gonads
Section 2 5. Systemic Lupus Erythematosus 6. Rheumatoid Disease and Other Inflammatory Arthropathies 7. Amyloidosis and Other Protein Deposition Diseases 8. Immunodeficiency Disorders 9. Inherited Complement Deficiencies 10. Inflammatory Disorders 11. Celiac Disease 12. Disorders of Leukocyte Function
Section 3 13. Genetic Disorders of the Pituitary Gland 14. Thyroid Disorders 15. Parathyroid Disorders, 16. Diabetes Mellitus 17. Genetic Disorders of the Adrenal Gland 18. Disorders of the Gonads
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ADPKD; APOL1; ARPKD; Autoimmune; Bacterial infections; Complement; Congenital anomalies; Cystic disorders; Cystinuria; Cysts; Distal renal tubular acidosis; Fanconi syndrome; FSGS; Genetic kidney disease; Hemoglobin; Hemoglobinopathies; Hemolytic uremic syndrome; Histocompatibility; HLA; Hypophosphatemic rickets; Immune response; Kidney; Kidney development; Meningitis; Monogenic kidney disease; Nephrotic syndrome; Next-generation sequencing; NPHS1; NPHS2; Proximal renal tubular acidosis; Renal developmental pathways; Rheumatoid arthritis; Sickle cell disease; Systemic lupus erythematosus; Thalassemia; Tuberous sclerosis; WT1
Section 1 1. Hemoglobinopathies and Thalassemias 2. Other Hereditary Red Blood Cell Disorders 3. Hemophilias and Other Disorders of Hemostasis 4. Rhesus and Other Fetomaternal Incompatibilities
Section 2 5. Systemic Lupus Erythematosus 6. Rheumatoid Disease and Other Inflammatory Arthropathies 7. Amyloidosis and Other Protein Deposition Diseases 8. Immunodeficiency Disorders 9. Inherited Complement Deficiencies 10. Inflammatory Disorders 11. Celiac Disease 12. Disorders of Leukocyte Function
Section 3 13. Genetic Disorders of the Pituitary Gland 14. Thyroid Disorders 15. Parathyroid Disorders, 16. Diabetes Mellitus 17. Genetic Disorders of the Adrenal Gland 18. Disorders of the Gonads
Section 2 5. Systemic Lupus Erythematosus 6. Rheumatoid Disease and Other Inflammatory Arthropathies 7. Amyloidosis and Other Protein Deposition Diseases 8. Immunodeficiency Disorders 9. Inherited Complement Deficiencies 10. Inflammatory Disorders 11. Celiac Disease 12. Disorders of Leukocyte Function
Section 3 13. Genetic Disorders of the Pituitary Gland 14. Thyroid Disorders 15. Parathyroid Disorders, 16. Diabetes Mellitus 17. Genetic Disorders of the Adrenal Gland 18. Disorders of the Gonads
Este título pertence ao(s) assunto(s) indicados(s). Para ver outros títulos clique no assunto desejado.
ADPKD; APOL1; ARPKD; Autoimmune; Bacterial infections; Complement; Congenital anomalies; Cystic disorders; Cystinuria; Cysts; Distal renal tubular acidosis; Fanconi syndrome; FSGS; Genetic kidney disease; Hemoglobin; Hemoglobinopathies; Hemolytic uremic syndrome; Histocompatibility; HLA; Hypophosphatemic rickets; Immune response; Kidney; Kidney development; Meningitis; Monogenic kidney disease; Nephrotic syndrome; Next-generation sequencing; NPHS1; NPHS2; Proximal renal tubular acidosis; Renal developmental pathways; Rheumatoid arthritis; Sickle cell disease; Systemic lupus erythematosus; Thalassemia; Tuberous sclerosis; WT1