nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Bone marrow transplantation for the treatment of genetic diseases
|
Cowan, Morton J. |
|
1991 |
24 |
4 |
p. 375-381 7 p. |
artikel |
2 |
Cystic fibrosis gene analysis: recent diagnostic applications
|
Fujimura, Frank K. |
|
1991 |
24 |
4 |
p. 353-361 9 p. |
artikel |
3 |
Detection of hereditary metabolic disorders involving amino acids and organic acids
|
Shih, Vivian E. |
|
1991 |
24 |
4 |
p. 301-309 9 p. |
artikel |
4 |
Evaluation of carbonic anhydrase isozymes in disorders involving osteopetrosis and/or renal tubular acidosis
|
Sly, William S. |
|
1991 |
24 |
4 |
p. 311-318 8 p. |
artikel |
5 |
Foreword
|
Sherwin, John E. |
|
1991 |
24 |
4 |
p. 289- 1 p. |
artikel |
6 |
Galactosemia: screening and diagnosis
|
Beutler, Ernest |
|
1991 |
24 |
4 |
p. 293-300 8 p. |
artikel |
7 |
Inborn errors of fatty acid oxidation in man
|
Rhead, William J. |
|
1991 |
24 |
4 |
p. 319-329 11 p. |
artikel |
8 |
Laboratory diagnosis of hemoglobinopathies
|
Lubin, Bertram H. |
|
1991 |
24 |
4 |
p. 363-374 12 p. |
artikel |
9 |
Lactic acidosis and mitochondrial disorders
|
Kerr, Douglas S. |
|
1991 |
24 |
4 |
p. 331-336 6 p. |
artikel |
10 |
National Academy of Clinical Biochemistry: Kodak Lectureship Award recipient
|
|
|
1991 |
24 |
4 |
p. 291- 1 p. |
artikel |
11 |
Peroxisomal disorders
|
Moser, Hugo W. |
|
1991 |
24 |
4 |
p. 343-351 9 p. |
artikel |
12 |
Phenylketonuria: screening, treatment and maternal PKU
|
Matalon, Reuben |
|
1991 |
24 |
4 |
p. 337-342 6 p. |
artikel |