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- 2007
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Mark
CDG-Id in two siblings with partially different phenotypes
(
- Contribution to journal › Article
- 2005
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Mark
PTPN11 mutations play a minor role in isolated congenital heart disease
(
- Contribution to journal › Article
-
Mark
Human neuropeptide Y signal peptide gain-of-function polymorphism is associated with increased body mass index : possible mode of function
(
- Contribution to journal › Article
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Mark
Clinical and molecular characterization of the first adult congenital disorder of glycosylation (CDG) type Ic patient
(
- Contribution to journal › Article
- 2004
-
Mark
One in 10 ovarian cancer patients carry germ line BRCA1 or BRCA2 mutations : results of a prospective study in Southern Sweden
(
- Contribution to journal › Article
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Mark
Susceptibility to Paget's disease of bone is influenced by a common polymorphic variant of osteoprotegerin
(
- Contribution to journal › Article
- 2002
-
Mark
Molecular genetic characterization of the EWS/ATF1 fusion gene in clear cell sarcoma of tendons and aponeuroses.
(
- Contribution to journal › Article
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Mark
Cytogenetic aberrations and heterogeneity of mutations in repeat-containing genes in a colon carcinoma from a patient with hereditary nonpolyposis colorectal cancer.
(
- Contribution to journal › Article
- 2001
-
Mark
Predictive genetic screening and clinical findings in multiple endocrine neoplasia type I families
(
- Contribution to journal › Article
- 1999
-
Mark
hMLH1, hMSH2 and hMSH6 mutations in hereditary non-polyposis colorectal cancer families from southern Sweden
(
- Contribution to journal › Article