161 – 170 of 278
- show: 10
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2008
-
Mark
CHD7 mutation spectrum in 28 Swedish patients diagnosed with CHARGE syndrome
(
- Contribution to journal › Article
-
Mark
Role of homologous recombination in trabectedin-induced DNA damage
(
- Contribution to journal › Article
-
Mark
Infertility, treatment of infertility, and the risk of breast cancer among women with BRCA1 and BRCA2 mutations : a case-control study
(
- Contribution to journal › Article
- 2007
-
Mark
Genomic profiling of malignant melanoma using tiling-resolution arrayCGH.
(
- Contribution to journal › Article
-
Mark
Comprehensive mutational analysis of a cohort of Swedish Cornelia de Lange syndrome patients
(
- Contribution to journal › Article
-
Mark
Expression and mutation analysis of the discoidin domain receptors 1 and 2 in non-small cell lung carcinoma.
(
- Contribution to journal › Article
-
Mark
C1q deficiency in an Inuit family: Identification of a new class of C1q disease-causing mutations
(
- Contribution to journal › Article
-
Mark
Confirmation of a BRAF mutation-associated gene expression signature in melanoma
(
- Contribution to journal › Article
-
Mark
The genetics of congenital heart disease : a review of recent developments
(
- Contribution to journal › Scientific review
-
Mark
Identification, expression, and functional analyses of a thylakoid ATP/ADP carrier from Arabidopsis
(
- Contribution to journal › Article