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Genetics, Medical. --- Genetic Diseases, Inborn. --- 575.21 --- Human chromosomes --- -Medical genetics --- -Clinical genetics --- Diseases --- Heredity of disease --- Human genetics --- Medical sciences --- Pathology --- Genetic disorders --- Chromosomes --- 575.21 Phenotypic variation. Phenotype --- Phenotypic variation. Phenotype --- Genetic Diseases --- Genetic Disorders --- Hereditary Disease --- Inborn Genetic Diseases --- Single-Gene Defects --- Hereditary Diseases --- Defect, Single-Gene --- Defects, Single-Gene --- Disease, Genetic --- Disease, Hereditary --- Disease, Inborn Genetic --- Diseases, Genetic --- Diseases, Hereditary --- Diseases, Inborn Genetic --- Disorder, Genetic --- Disorders, Genetic --- Genetic Disease --- Genetic Disease, Inborn --- Genetic Disorder --- Inborn Genetic Disease --- Single Gene Defects --- Single-Gene Defect --- Genetics, Medical --- Human Genetics --- Medical Genetics --- Genetics, Human --- Anthropology, Physical --- Chromosome Disorders --- Sex Chromosome Disorders --- Genetic Diseases, Inborn --- Molecular Medicine --- Bibliography --- Dictionaries --- Genetic aspects --- -575.21 Phenotypic variation. Phenotype --- Clinical genetics --- Medical genetics
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Clinical genetics --- Medical genetics --- Genetic Diseases, Inborn --- Genetics, Medical --- Diseases --- Heredity of disease --- Human genetics --- Medical sciences --- Pathology --- Genetic disorders --- Medical Genetics --- Anthropology, Physical --- Chromosome Disorders --- Sex Chromosome Disorders --- Molecular Medicine --- Genetic Diseases --- Genetic Disorders --- Hereditary Disease --- Inborn Genetic Diseases --- Single-Gene Defects --- Hereditary Diseases --- Defect, Single-Gene --- Defects, Single-Gene --- Disease, Genetic --- Disease, Hereditary --- Disease, Inborn Genetic --- Diseases, Genetic --- Diseases, Hereditary --- Diseases, Inborn Genetic --- Disorder, Genetic --- Disorders, Genetic --- Genetic Disease --- Genetic Disease, Inborn --- Genetic Disorder --- Inborn Genetic Disease --- Single Gene Defects --- Single-Gene Defect --- Genetic aspects --- Genetics, Medical. --- Medical genetics.
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Pathological haematology --- Blood Group Antigens. --- Disease --- Disease. --- Polymorphism, Genetic. --- Blood groups --- Diseases --- -Genetic polymorphisms --- Medical genetics --- Clinical genetics --- Heredity of disease --- Human genetics --- Medical sciences --- Pathology --- Genetic disorders --- Polymorphisms, Genetic --- Population genetics --- Human beings --- Illness --- Illnesses --- Morbidity --- Sickness --- Sicknesses --- Medicine --- Epidemiology --- Health --- Sick --- Blood --- Blood types --- Groups, Blood --- Types, Blood --- Heredity --- Physical anthropology --- Paternity testing --- Genetic Polymorphisms --- Genetic Polymorphism --- Polymorphism (Genetics) --- Blood Groups --- Antigens, Blood Group --- Isoantibodies --- etiology. --- Causes and theories of causation --- Genetic aspects --- Groups --- Examination --- Agglutination --- Transfusion --- Blood groups. --- Genetic polymorphisms. --- Medical genetics. --- Causes and theories of causation. --- Antigens, CD44 --- Genetic polymorphisms --- Blood Group Antigens --- Polymorphism, Genetic --- Polymorphisms (Genetics) --- Hyaluronan Receptors --- Aetiology --- Etiology --- etiology --- Gene Polymorphism --- Gene Polymorphisms --- Polymorphism, Gene --- Polymorphisms, Gene --- Blood Group --- Blood Group Antigen --- Antigen, Blood Group --- Group Antigen, Blood --- Group, Blood
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