Hereditary Books
Normal red blood cells - membrane cytoskeleton ,overview of RBC disorders
Author: AN Duru
School: University of Nigeria, Nsukka
Department: Medical, Pharmaceutical and Health science
Course Code: HEM301
Topics: RBC Function, RBC membrane, RBC membrane protein, Glycophorin, Spectrin, integral membrane proteins, peripheral proteins, red cell membrane lipids, Phospholipids, Glycolipids, Cholesterol, RBC membrane disorders, Hereditary spherocytosis, Hereditary elliptocytosis, Hereditary pyropoikilocytosis, Hereditary Stomatocytosis Syndromes, Overhydrated Hereditary Stomatocytosis, Dehydrated Hereditary Stomatocytosis
Haemolytic anemias , membrane disorders
Author: Haematology
School: University of Ilorin
Department: Medical, Pharmaceutical and Health science
Course Code: HAEMATOLOGY
Topics: Membrane disorders, MEMBRANOPATHIES, Red cell membrane, hereditary membrane disorders, Hereditary SpherocytosisAplastic crisis, Acute sequestration crisis, Megaloblastic crisis, Gallstones, Hereditary Elliptocytosis, Familial Lecithin-Cholesterol Acyl transferase Deficiency, Echinocytosis, Acanthocytosis, Abetalipoproteinaemia
Hereditary bleeding disorders, Haemophilia
Author: AO Shittu
School: University of Ilorin
Department: Medical, Pharmaceutical and Health science
Course Code: HAEMATOLOGY
Topics: Haemophilia B, Haemophilia A, Von-Willibrand disease, coagulation
Haemolytic anemias 2 , membrane disorders
Author: AO Shittu
School: University of Ilorin
Department: Medical, Pharmaceutical and Health science
Course Code: HAEMATOLOGY
Topics: red cell membrane, Protein-Membrane, HEREDITARY SPHEROCYTOSIS, OSMOTIC FRAGILITY TEST, ACIDIFIED GLYCEROL LYSIS TEST, AUTO HAEMOLYSIS, HEREDITARY ELLIPTOCYTOSIS, membrane lipids, Familial Lecithin, Cholesterol Acyltransferase Deficiency, lipoproteinaemia, Echinocytosis, Echinocytes, Acanthocytosis, Acanthocytes
Author: Morbid Anatomy
School: University of Ilorin
Department: Medical, Pharmaceutical and Health science
Course Code: MORBID ANATOMY
Topics: Benign neoplasms, Renal Papillary Adenoma, Wilms Tumour, Nephroblastoma, WAGR syndrome, Denys-Drash syndrome, Beckwith-Wiedemann Syndrome, Renal cell carcinoma, Von Hippel-Lindau syndrome, Hereditary leiomyomatosis, renal cell cancer syndrome, Hereditary papillary carcinoma, Birt-Hogg-Dubé Syndrome, Clear cell variant, Papillary variant, Xp11 translocation carcinoma, Collecting duct carcinoma, Bellini duct carcinoma, Medullary carcinoma
Chromosomes Genes & genetic diseases
Author: DB Olusina
School: University of Nigeria, Nsukka
Department: Medical, Pharmaceutical and Health science
Course Code: PAT301
Topics: DNA split, human karyogram, mutation, Genetic disorder, CYTOGENETIC DISORDER, AUTOSOMAL CYTOGENETIC DISORDER, down syndrome, EDWARD SYNDROME, PATAU SYNDROME, Lyonization, X-chromosome, Y-chromosome, Klinefelter's Syndrome, Testicular Dysgenesis, Male hypogonadism, Klinefelter Syndrome, Turner Syndrome, MENDELIAN DISORDER, Autosomal Dominant Disorder, Marfan Syndrome, Achondroplasia, Osteogenesis imperfecta, brittle bone disease, Ehlers-Danlos Syndrome, Autosomal recessive disorder, X-LINKED DISORDER, Multifactorial disorder, Hereditary Cancer Syndrome, DEFECTIVE DNA REPAIR, Single-Gene Disorder, TRIPLET-REPEAT MUTATION, FRAGILE-X SYNDROME, LEBER HEREDITARY OPTIC NEUROPATHY, GENOMIC IMPRINTING
Author: HJ Ozemoka
School: Edo University
Department: Science and Technology
Course Code: AEB111
Topics: Genetics, hereditary, classical genetics, molecular genetics, evolutionary genetics, Monohydrid inheritance
Author: Titilayo
School: Lagos State University
Department: Science and Technology
Course Code: BIO205
Topics: Genetic, hereditary, Gregor Mendel, Genetic terminology, Monohybrid crosses, patterns of inheritance, dihybrid crosses, test, cross, Mendelian Genetics, punnett square, Principle of Independent Assortment, incomplete dominance
Author: BIO UNIZIK
School: Nnamdi Azikiwe University
Department: Science and Technology
Course Code: BIO101
Topics: Biology, cellular biology, molecular biology, population biology, branches of biology, botany, cell, ecology, genetics, scientific methods, cell structure, prokaryotic cells, Eukaryotic cells, Eukaryotic plant cells, cell functions, movement, photosynthesis, protein synthesis, cell division, dark reaction, autotroph, heterotroph, parasitism, saprophytism, homeostasis, hereditary, evolution, living things, transport, response, coordination, reflex action, enzymes, hormones, nutrition, digestion, excretion, urine formation, filtration, reabsorption, Tubular secretion, metabolism, respiration, respiratory system, cell chemistry, carbohydrate, parasitism, parasite
IRON DEFICIENCY ANAEMIA AND HAEMOCHROMATOSIS
Author: Lawal
School: University of Ilorin
Department: Medical, Pharmaceutical and Health science
Course Code: BCH300
Topics: IRON DEFICIENCY ANAEMIA, HAEMOCHROMATOSIS, iron Distribution, Iron Storage, Iron overload, Hereditary heamochromatosis
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