| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
A method for sex assignment in mixed samples
|
Falconi, Mirella
|
|
2001
|
108 |
3 |
p. 267-268
|
article
|
| 2 |
Analysis of the CC chemokine receptor 5 (CCR5) delta-32 polymorphism in inflammatory bowel disease
|
Rector, Annabel
|
|
2001
|
108 |
3 |
p. 190-193
|
article
|
| 3 |
A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH)
|
Nietzel, Angela
|
|
2001
|
108 |
3 |
p. 199-204
|
article
|
| 4 |
A single nucleotide polymorphism (SNP) in the leptin receptor is associated with BMI, fat mass and leptin levels in postmenopausal Caucasian women
|
Quinton, Naomi
|
|
2001
|
108 |
3 |
p. 233-236
|
article
|
| 5 |
Carrier rate of APC I1307K is not increased in inflammatory bowel disease patients of Ashkenazi Jewish origin
|
Silverberg, Mark
|
|
2001
|
108 |
3 |
p. 205-210
|
article
|
| 6 |
CFTR gene mutations – including three novel nucleotide substitutions – and haplotype background in patients with asthma, disseminated bronchiectasis and chronic obstructive pulmonary disease
|
Tzetis, Maria
|
|
2001
|
108 |
3 |
p. 216-221
|
article
|
| 7 |
Characterisation of SMN hybrid genes in Spanish SMA patients: de novo, homozygous and compound heterozygous cases
|
Cuscó, Ivon
|
|
2001
|
108 |
3 |
p. 222-229
|
article
|
| 8 |
Complex segregation analysis of Parkinson's disease in the Finnish population
|
Moilanen, J.
|
|
2001
|
108 |
3 |
p. 184-189
|
article
|
| 9 |
Cross-sectional study on cytokine polymorphisms, cytokine production after T-cell stimulation and clinical parameters in a random sample of a German population
|
Nieters, Alexandra
|
|
2001
|
108 |
3 |
p. 241-248
|
article
|
| 10 |
De novo mutation of the connexin 26 gene associated with dominant non-syndromic sensorineural hearing loss
|
Janecke, Andreas R
|
|
2001
|
108 |
3 |
p. 269-270
|
article
|
| 11 |
Elite swimmers and the D allele of the ACE I/D polymorphism
|
Woods, David
|
|
2001
|
108 |
3 |
p. 230-232
|
article
|
| 12 |
Genomic organization, chromosomal localization, alternative splicing, and isoforms of the human synaptosome-associated protein-23 gene implicated in vesicle-membrane fusion processes
|
Lazo, Pedro
|
|
2001
|
108 |
3 |
p. 211-215
|
article
|
| 13 |
Increased reproductive success of MHC class II heterozygous males among free-ranging rhesus macaques
|
Sauermann, Ulrike
|
|
2001
|
108 |
3 |
p. 249-254
|
article
|
| 14 |
Mitochondrial DNA haplogroups and APOE4 allele are non-independent variables in sporadic Alzheimer's disease
|
Carrieri, Giuseppina
|
|
2001
|
108 |
3 |
p. 194-198
|
article
|
| 15 |
Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes
|
Neerman-Arbez, M.
|
|
2001
|
108 |
3 |
p. 237-240
|
article
|
| 16 |
SMN gene duplication and the emergence of the SMN2 gene occurred in distinct hominids: SMN2 is unique to Homo sapiens
|
Rochette, C.
|
|
2001
|
108 |
3 |
p. 255-266
|
article
|
| 17 |
The missense Glu298Asp variant of the endothelial nitric oxide synthase gene is strongly associated with placental abruption
|
Yoshimura, Toshihiro
|
|
2001
|
108 |
3 |
p. 181-183
|
article
|
Journal description