[Molecular disease].
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Hematologic Diseases↗
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Results for “METABOLIC DISEASES/genetics”
Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.
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Clinical manifestations of genetic aberrations of calcium and phosphorus metabolism.
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Calcium↗
Familial aminoaciduria in osteogenesis imperfecta.
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Amino Acids↗
[Familial Mediterranean fever. A genetically determined disease associated with amyloidosis].
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Amyloidosis↗
Hereditary absence of muscle phosphorylase (McArdle's syndrome).
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Glycogen Storage Disease Type V↗
The normal human female as a mosaic of X-chromosome activity: studies using the gene for C-6-PD-deficiency as a marker.
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Biomarkers↗
Biochemical genetics as illustrated by hereditary galactosemia.
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Galactose↗
Galactosemia: a study of twenty-seven kindreds in North America.
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Galactose↗
Genetic errors of metabolism and environmental interaction: a synthesis.
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Environment↗
Hypophosphatasia: a genetic study.
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Humans↗
The inheritance of essential pentosuria.
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Carbohydrate Metabolism, Inborn Errors↗
A survey of some hereditary metabolic diseases.
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Data Collection↗
Inborn errors of carbohydrate metabolism.
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Carbohydrate Metabolism↗
Inherited enzyme disorders. A new and expanding area of far-reaching significance.
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Enzymes↗
The metabolic basis of some inborn intellectual disorders in adolescents.
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Adolescent↗
[Symposium on metabolic diseases of genetic orgin. Introduction].
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Humans↗
Acanthrocytosis, pigmentary degeneration of the retina and ataxic neuropathy: a genetically determined syndrome and associated metabolic disorder.
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Congenital Abnormalities↗