| 000 | 01329cam a2200241 4500 | ||
|---|---|---|---|
| 001 | 0071363203 | ||
| 008 | 101203t2001 xxu||||| |||| 00| 0 eng d | ||
| 020 | _a0071363203 | ||
| 100 | _aScriver, C.R. (ed) | ||
| 245 | 4 | _aThe metabolic and molecular bases of inherited disease volume II | |
| 250 | _a8th | ||
| 260 |
_aNew York _bMcGraw-Hill _c2001 |
||
| 300 | _a1665-3368; ill.,bibls.; BookFind | ||
| 505 | _aAmino acids; organic acids; disorders of mitochondrial function; purines and pyrimidines; lipids; porphyrins; metals; peroxisomes. | ||
| 520 | _aHardback | ||
| 520 | _aThis 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. | ||
| 650 | _aGENETIC DISEASES, INBORN | ||
| 650 |
_aMETABOLIC DISEASES _96981 |
||
| 650 |
_aMETABOLISM, INBORN ERRORS _96983 |
||
| 700 | _aBeaudet, A.L. (ed) | ||
| 700 | _aSly, W.S. (ed) | ||
| 700 | _aValle, D. (ed) | ||
| 999 |
_c80528 _d80528 |
||