Samuel Gebre-Medhin
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- 2017
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Mark
Expanding the genotype–phenotype spectrum in hereditary colorectal cancer by gene panel testing
(
- Contribution to journal › Article
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Mark
Corticotroph Pituitary Carcinoma in a Patient With Lynch Syndrome (LS) and Pituitary Tumors in a Nationwide LS Cohort
(
- Contribution to journal › Article
-
Mark
Genetic anticipation in Swedish Lynch syndrome families
(
- Contribution to journal › Article
- 2016
-
Mark
L1 syndrome diagnosis complemented with functional analysis of L1CAM variants located to the two N-terminal Ig-like domains.
2016) In Clinical Genetics(
- Contribution to journal › Article
-
Mark
Phenotype and genotype in 52 patients with Rubinstein–Taybi syndrome caused by EP300 mutations
(
- Contribution to journal › Article
- 2012
-
Mark
Food intake and meal pattern in IAPP knockout mice with and without infusion of exogenous IAPP
(
- Contribution to journal › Article
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Mark
Recurrent Rearrangement of the PHF1 Gene in Ossifying Fibromyxoid Tumors.
(
- Contribution to journal › Article
- 2009
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Mark
Telomeric associations correlate with telomere length reduction and clonal chromosome aberrations in giant cell tumor of bone.
(
- Contribution to journal › Article
- 2004
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Mark
Amylin inhibits bone resorption while the calcitonin receptor controls bone formation in vivo
(
- Contribution to journal › Article
- 2003
-
Mark
Consequences of eliminating adenosine A(1) receptors in mice
(
- Chapter in Book/Report/Conference proceeding › Paper in conference proceeding