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- 2008
-
Mark
Independent introduction of two lactase-persistence alleles into human populations reflects different history of adaptation to milk culture
(
- Contribution to journal › Article
-
Mark
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans
(
- Contribution to journal › Article
-
Mark
Identification of ten loci associated with height highlights new biological pathways in human growth
(
- Contribution to journal › Article
-
Mark
Common Missense Variant in the Glucokinase Regulatory Protein Gene Is Associated With Increased Plasma Triglyceride and C-Reactive Protein but Lower Fasting Glucose Concentrations
(
- Contribution to journal › Article
- 2007
-
Mark
Evidence of still-ongoing convergence evolution of the lactase persistence T-13910 alleles in humans
(
- Contribution to journal › Article
-
Mark
A common variant of HMGA2 is associated with adult and childhood height in the general population
(
- Contribution to journal › Article
- 2002
-
Mark
ABCB6 (MTABC3) excluded as the causative gene for the growth retardation syndrome with aminoaciduria, cholestasis, iron overload, and lactacidosis
(
- Contribution to journal › Article
-
Mark
Antenatal diagnosis of hereditary fetal growth retardation with aminoaciduria, cholestasis, iron overload, and lactic acidosis in the newborn infant
(
- Contribution to journal › Article
-
Mark
GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCS1L
(
- Contribution to journal › Article
- 1994
-
Mark
An extra cysteine in one of the non calcium binding EGF-like motifs of the FBN1 polypeptide is connected to a novel variant of Marfan syndrome
(
- Contribution to journal › Article
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