nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A genome-wide survey of human thioredoxin and glutaredoxin family pseudogenes
|
Spyrou, Giannis |
|
2001 |
109 |
4 |
p. 429-439 |
artikel |
2 |
A genome-wide survey of human thioredoxin and glutaredoxin family pseudogenes
|
Spyrou, Giannis |
|
2001 |
109 |
4 |
p. 429-439 |
artikel |
3 |
Announcement
|
|
|
2001 |
109 |
4 |
p. 468-469 |
artikel |
4 |
Announcement
|
|
|
2001 |
109 |
4 |
p. 470 |
artikel |
5 |
Chromosome 17 and the inducible nitric oxide synthase gene in human essential hypertension
|
Rutherford, Sue |
|
2001 |
109 |
4 |
p. 408-415 |
artikel |
6 |
Chromosome 17 and the inducible nitric oxide synthase gene in human essential hypertension
|
Rutherford, Sue |
|
2001 |
109 |
4 |
p. 408-415 |
artikel |
7 |
Genetic predisposition to ventricular septal defect in Down syndrome
|
Marino, Bruno |
|
2001 |
109 |
4 |
p. 463 |
artikel |
8 |
Genetic risk factors of venous thrombosis
|
Franco, Rendrik F. |
|
2001 |
109 |
4 |
p. 369-384 |
artikel |
9 |
Genetic risk factors of venous thrombosis
|
Franco, Rendrik F. |
|
2001 |
109 |
4 |
p. 369-384 |
artikel |
10 |
Helmut Schenkel-Brunner: Human blood groups: chemical and biological basis of antigen, 2nd edn., Springer-Verlag, Wien New York. ISBN 3-211-83471-0. DM 198.–, US$ 99.0. Hardcover, 637 pages
|
Reid, Marion E. |
|
2001 |
109 |
4 |
p. 465 |
artikel |
11 |
Helmut Schenkel-Brunner: Human blood groups: chemical and biological basis of antigen, 2nd edn., Springer-Verlag, Wien New York. ISBN 3-211-83471-0. DM 198.–, US$ 99.0. Hardcover, 637 pages
|
Reid, Marion E. |
|
2001 |
109 |
4 |
p. 465 |
artikel |
12 |
Identification of 96 single nucleotide polymorphisms in eight genes involved in iron metabolism: efficiency of bioinformatic extraction compared with a systematic sequencing approach
|
Douabin-Gicquel, Véronique |
|
2001 |
109 |
4 |
p. 393-401 |
artikel |
13 |
Identification of 96 single nucleotide polymorphisms in eight genes involved in iron metabolism: efficiency of bioinformatic extraction compared with a systematic sequencing approach
|
Douabin-Gicquel, Véronique |
|
2001 |
109 |
4 |
p. 393-401 |
artikel |
14 |
Long mutant dystrophins and variable phenotypes: evasion of nonsense-mediated decay?
|
Kerr, Tim P. |
|
2001 |
109 |
4 |
p. 402-407 |
artikel |
15 |
Long mutant dystrophins and variable phenotypes: evasion of nonsense-mediated decay?
|
Kerr, Tim P. |
|
2001 |
109 |
4 |
p. 402-407 |
artikel |
16 |
Marfan syndrome caused by a mutation in FBN1 that gives rise to cryptic splicing and a 33 nucleotide insertion in the coding sequence
|
Hutchinson, Sarah |
|
2001 |
109 |
4 |
p. 416-420 |
artikel |
17 |
Marfan syndrome caused by a mutation in FBN1 that gives rise to cryptic splicing and a 33 nucleotide insertion in the coding sequence
|
Hutchinson, Sarah |
|
2001 |
109 |
4 |
p. 416-420 |
artikel |
18 |
Muscular Dystrophy: methods and protocols
|
Roberts, Roland G. |
|
2001 |
109 |
4 |
p. 466-467 |
artikel |
19 |
Physical activity modulates the combined effect of a common variant of the lipoprotein lipase gene and smoking on serum triglyceride levels and high-density lipoprotein cholesterol in men
|
Sentí, Mariano |
|
2001 |
109 |
4 |
p. 385-392 |
artikel |
20 |
Physical activity modulates the combined effect of a common variant of the lipoprotein lipase gene and smoking on serum triglyceride levels and high-density lipoprotein cholesterol in men
|
Sentí, Mariano |
|
2001 |
109 |
4 |
p. 385-392 |
artikel |
21 |
Prenatal diagnosis and fetal pathology in a Turkish family harboring a novel nonsense mutation in the lysosomal α-N-acetyl-neuraminidase (sialidase) gene
|
Sergi, Consolato |
|
2001 |
109 |
4 |
p. 421-428 |
artikel |
22 |
Prenatal diagnosis and fetal pathology in a Turkish family harboring a novel nonsense mutation in the lysosomal α-N-acetyl-neuraminidase (sialidase) gene
|
Sergi, Consolato |
|
2001 |
109 |
4 |
p. 421-428 |
artikel |
23 |
Satellite 2 methylation patterns in normal and ICF syndrome cells and association of hypomethylation with advanced replication
|
Hassan, Anwarul K. |
|
2001 |
109 |
4 |
p. 452-462 |
artikel |
24 |
Satellite 2 methylation patterns in normal and ICF syndrome cells and association of hypomethylation with advanced replication
|
Hassan, Anwarul K. |
|
2001 |
109 |
4 |
p. 452-462 |
artikel |
25 |
Subtelomeric rearrangements: results from a study of selected and unselected probands with idiopathic mental retardation and control individuals by using high-resolution G-banding and FISH
|
Joyce, C. |
|
2001 |
109 |
4 |
p. 440-451 |
artikel |
26 |
Subtelomeric rearrangements: results from a study of selected and unselected probands with idiopathic mental retardation and control individuals by using high-resolution G-banding and FISH
|
Joyce, C. |
|
2001 |
109 |
4 |
p. 440-451 |
artikel |
27 |
Suomi-Neidon Geenit (The Genes of Maiden Finland)
|
Harper, Peter S. |
|
2001 |
109 |
4 |
p. 464 |
artikel |