The metabolic and molecular bases of inherited disease volume II
Scriver, C.R. (ed)
The metabolic and molecular bases of inherited disease volume II - 8th - New York McGraw-Hill 2001 - 1665-3368; ill.,bibls.; BookFind
Amino acids; organic acids; disorders of mitochondrial function; purines and pyrimidines; lipids; porphyrins; metals; peroxisomes.
Hardback This is a reference guide for information in the field of molecular biology. It covers areas such as, the effects of genes, their location on the chromosomes and what treatment, if any, can be recommended to paediatricians and other clinicians whose patients show certain signs and symptoms. This eighth edition has been expanded and updated to include colon cancer, breast cancer, triplet repeat disorders, fragile X mental retardation, biochemical and molecular mechanisms, and clinical diagnosis and management approaches.
0071363203
GENETIC DISEASES, INBORN
METABOLIC DISEASES
METABOLISM, INBORN ERRORS
The metabolic and molecular bases of inherited disease volume II - 8th - New York McGraw-Hill 2001 - 1665-3368; ill.,bibls.; BookFind
Amino acids; organic acids; disorders of mitochondrial function; purines and pyrimidines; lipids; porphyrins; metals; peroxisomes.
Hardback This is a reference guide for information in the field of molecular biology. It covers areas such as, the effects of genes, their location on the chromosomes and what treatment, if any, can be recommended to paediatricians and other clinicians whose patients show certain signs and symptoms. This eighth edition has been expanded and updated to include colon cancer, breast cancer, triplet repeat disorders, fragile X mental retardation, biochemical and molecular mechanisms, and clinical diagnosis and management approaches.
0071363203
GENETIC DISEASES, INBORN
METABOLIC DISEASES
METABOLISM, INBORN ERRORS