| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
ABCA1 gene polymorphisms and their associations with coronary artery disease and plasma lipids in males from three ethnic populations in Singapore
|
Tan, Jenny Hui-Hui
|
|
2003
|
113 |
2 |
p. 106-117
|
artikel
|
| 2 |
A deletion in the human QP-C gene causes a complex III deficiency resulting in hypoglycaemia and lactic acidosis
|
Haut, Sandrine
|
|
2003
|
113 |
2 |
p. 118-122
|
artikel
|
| 3 |
Bone dysplasias: an atlas of genetic disorders of skeletal development, 2nd edition
|
Young, Ian D.
|
|
2003
|
113 |
2 |
p. 194
|
artikel
|
| 4 |
Cis-acting variation in the expression of a high proportion of genes in human brain
|
Bray, Nicholas J.
|
|
2003
|
113 |
2 |
p. 149-153
|
artikel
|
| 5 |
Common 5′ β-globin RFLP haplotypes harbour a surprising level of ancestral sequence mosaicism
|
Webster, Matthew T.
|
|
2003
|
113 |
2 |
p. 123-139
|
artikel
|
| 6 |
David J. Galas, Stephen J. McCormack (eds): Genomic Technologies — Present and Future. Functional Genomics Series, Vol 1 (Series ed: Milton H. Saier Jr)
|
Dear, Paul
|
|
2003
|
113 |
2 |
p. 193
|
artikel
|
| 7 |
Disruption of exon definition produces a dominant-negative growth hormone isoform that causes somatotroph death and IGHD II
|
Ryther, Robin C. C.
|
|
2003
|
113 |
2 |
p. 140-148
|
artikel
|
| 8 |
Hyaluronan is not elevated in urine or serum in Hutchinson-Gilford Progeria Syndrome
|
Gordon, Leslie B.
|
|
2003
|
113 |
2 |
p. 178-187
|
artikel
|
| 9 |
Interphase FISH, the structure of reciprocal translocation chromosomes and physical mapping studies rule out the duplication of the NF1 gene at 17q11.2. A reply
|
Kehrer-Sawatzki, Hildegard
|
|
2003
|
113 |
2 |
p. 188-190
|
artikel
|
| 10 |
Linkage and association mapping of the LRP5 locus on chromosome 11q13 in type 1 diabetes
|
Twells, Rebecca C. J.
|
|
2003
|
113 |
2 |
p. 99-105
|
artikel
|
| 11 |
Methods in molecular biology, vol 204. Molecular cytogenetics: protocols and applications
|
Crolla, John A.
|
|
2003
|
113 |
2 |
p. 191-192
|
artikel
|
| 12 |
Mucopolysaccharidosis IVA: characterization of a common mutation found in Finnish patients with attenuated phenotype
|
Montaño, Adriana Maria
|
|
2003
|
113 |
2 |
p. 162-169
|
artikel
|
| 13 |
SONIC HEDGEHOG mutations causing human holoprosencephaly impair neural patterning activity
|
Schell-Apacik, Can
|
|
2003
|
113 |
2 |
p. 170-177
|
artikel
|
| 14 |
Translocation breakpoint in two unrelated Tourette syndrome cases, within a region previously linked to the disorder
|
Crawford, Fiona C.
|
|
2003
|
113 |
2 |
p. 154-161
|
artikel
|
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