11 – 19 of 19
- show: 10
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- « previous
- 1
- 2
- next »
- 2014
-
Mark
Identification of three novel FGF16 mutations in X-linked recessive fusion of the fourth and fifth metacarpals and possible correlation with heart disease.
(
- Contribution to journal › Article
-
Mark
Genome-wide association study and mouse expression data identify a highly conserved 32kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder.
(
- Contribution to journal › Article
- 2012
-
Mark
Genome-wide linkage analysis in families with infantile hypertrophic pyloric stenosis indicates novel susceptibility loci
(
- Contribution to journal › Article
- 2010
-
Mark
Livslång uppföljning krävs vid medfödd missbildning.
(
- Contribution to journal › Scientific review
-
Mark
22q11.2 microduplication in two patients with bladder exstrophy and hearing impairment
(
- Contribution to journal › Article
- 2006
-
Mark
Frequent finding of the androgen receptor A645D variant in normal population.
(
- Contribution to journal › Article
- 2005
-
Mark
The RsaI polymorphism in the ER{beta} gene is associated with male infertility.
(
- Contribution to journal › Article
- 2004
-
Mark
GENOME-WIDE LINKAGE ANALYSIS FOR HYPOSPADIAS SUSCEPTIBILITY GENES.
(
- Contribution to journal › Article
- 2002
-
Mark
An androgen receptor gene mutation (E653K) in a family with congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency as well as in partial androgen insensitivity.
(
- Contribution to journal › Article
- « previous
- 1
- 2
- next »