Haukur Örvar Pálmason, Moser, D, Sigmund, J, Vogler, C, Hänig, S, Schneider, A, ...
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Hunzelmann, N., Genth, E., Krieg, T., Lehmacher, W., Melchers, I., Meurer, M., ...
Objective. Systemic sclerosis (SSc) is a rare, heterogeneous disease, which affects different organs and therefore requires interdisciplinary diagnostic and therapeutic management. To improve the...
Association and linkage of allelic variants of the dopamine transporter gene in ADHD (2007)
Friedel, S., Saar, K., Sauer, S., Dempfle, A., Walitza, S., Renner, T., ...
Previously, we had reported a genome-wide scan for attention-deficit/hyperactivity disorder (ADHD) in 102 families with affected sibs of German ancestry; the highest multipoint LOD score of 4.75 was...
Association and linkage of allelic variants of the dopamine transporter gene in ADHD (2007)
Friedel, S., Saar, K., Sauer, S., Dempfle, A., Walitza, S., Renner, T., ...
Previously, we had reported a genome-wide scan for attention-deficit/hyperactivity disorder (ADHD) in 102 families with affected sibs of German ancestry; the highest multipoint LOD score of 4.75 was...
In situ Er-doping of SiC bulk single crystals (2004)
Müller, R., Desperrier, P., Seitz, C., Weisser, M., Magerl, A., Maier, M., ...
In this work the first PVT grown in-situ erbium doped SiC bulk crystal, to our knowledge, is presented. The crystal was characterised by secondary ion mass spectrometry (SIMS) and photoluminescence...
Genotypic and phenotypic spectrum in tricho-rhino-phalangeal syndrome types I and III (2001)
Schaper, J, Meinecke, P, Momeni, P, Gross, S, Von Holtum D, ...
Tricho-rhino-phalangeal syndrome (TRPS) is characterized by craniofacial and skeletal abnormalities. Three subtypes have been described: TRPS I, caused by mutations in the TRPS1 gene on chromosome 8;...
Utermann, G, Menzel, H J, Kraft, H G, Duba, H C, Kemmler, H G, Seitz, C
The Lp(a) lipoprotein represents a quantitative genetic trait. It contains two different polypeptide chains, the Lp(a) glycoprotein and apo B-100. We have demonstrated the Lp(a) glycoprotein directly...
Genotypic and Phenotypic Spectrum in Tricho-Rhino-Phalangeal Syndrome Types I and III
Schaper, J., Meinecke, P., Momeni, P., Groß, S., Von Holtum, D., ...
Tricho-rhino-phalangeal syndrome (TRPS) is characterized by craniofacial and skeletal abnormalities. Three subtypes have been described: TRPS I, caused by mutations in the TRPS1 gene on chromosome 8;...
Utermann, G, Menzel, H J, Kraft, H G, Duba, H C, Kemmler, H G, Seitz, C
The Lp(a) lipoprotein represents a quantitative genetic trait. It contains two different polypeptide chains, the Lp(a) glycoprotein and apo B-100. We have demonstrated the Lp(a) glycoprotein directly...
Genotypic and Phenotypic Spectrum in Tricho-Rhino-Phalangeal Syndrome Types I and III
Schaper, J., Meinecke, P., Momeni, P., Groß, S., Von Holtum, D., ...
Tricho-rhino-phalangeal syndrome (TRPS) is characterized by craniofacial and skeletal abnormalities. Three subtypes have been described: TRPS I, caused by mutations in the TRPS1 gene on chromosome 8;...
Hunzelmann, N., Genth, E., Krieg, T., Lehmacher, W., Melchers, I., Meurer, M., ...
Objective. Systemic sclerosis (SSc) is a rare, heterogeneous disease, which affects different organs and therefore requires interdisciplinary diagnostic and therapeutic management. To improve the...