( en | de | ru )

 

Disambiguation of "Ahnert, Peter"

Author of the publication

copydeleteadd this publication to your clipboard
Imaging genetics of FOXP2 in dyslexia

, , , , , , , , , , , , and . European journal of human genetics : EJHG, 20 (2): 224–229 (2012)

Please choose a person to relate this publication to

To differ between persons with the same name, the academic degree and the title of an important publication will be displayed. You can also use the button next to the name to display some publications already assigned to the person.

Manfred Ahnert

Lieselotte Ahnert

Gudrun Ahnert

Ahmed Ahnert

Helga Ahnert

 

Other publications of authors with the same name

Imaging genetics of FOXP2 in dyslexia, , , , , , , , , and 3 other author(s). European journal of human genetics : EJHG, 20 (2): 224–229 (2012)Bortezomib sensitizes primary human esthesioneuroblastoma cells to TRAIL-induced apoptosis, , , , , , , , , and 2 other author(s). Journal of neuro-oncology, 97 (2): 171–185 (2010)WHO grade-specific comparative genomic hybridization pattern of astrocytoma - a meta-analysis, , , , and . Pathology, research and practice, 206 (10): 663–668 (2010)Population-genetic comparison of the Sorbian isolate population in Germany with the German KORA population using genome-wide SNP arrays, , , , , , , , , and 4 other author(s). BMC genetics, (2011)Association study of a functional genetic variant in KIAA0319 in German dyslexics, , , , and . Psychiatric genetics, 22 (4): 216–217 (2012)The pore size of PLGA bone implants determines the de novo formation of bone tissue in tibial head defects in rats, , , , , , , , , and . Magnetic resonance in medicine : official journal of the Society of Magnetic Resonance in Medicine / Society of Magnetic Resonance in Medicine, 70 (4): 925–935 (2013)Association of rs2069459 in the CDK5 gene with dyslexia in a German cohort, , , , , , , , and . Psychiatric genetics, 22 (6): 307–308 (2012)Risk of tumorigenicity in mesenchymal stromal cell-based therapies--bridging scientific observations and regulatory viewpoints, , , , , , , , , and 9 other author(s). Cytotherapy, 15 (7): 753–759 (2013)The role of gene DCDC2 in German dyslexics, , , , , and . Annals of dyslexia, 59 (1): 1–11 (2009)CalcDalton: a tool for multiplex genotyping primer design for single-base extension reactions using cleavable primers, , , and . Biotechniques, 40 (2): 158, 160, 162 (2006)