E-LIB Suche - Ergebnisse für: Steiner-Weber, Astrid

1

Incidence of perinatal complications in children with prema..:

Weber, Benedikt ; Schwabegger, Anton H. ; Oberaigner, Wilhelm..
Journal of Perinatal Medicine. 38 (2010) 3 - p. , 2010

Link: https://doi.org/10.1515/..

2

Colour specificity in episodic and in perceptual object rec..:

Zimmer, Hubert ; Steiner, Astrid
European Journal of Cognitive Psychology. 15 (2003) 3 - p. 349-370 , 2003

Link: https://doi.org/10.1080/..

3

How "Implicit\ Are Implicit Color Effects in Memory?:

Zimmer, Hubert D. ; Steiner, Astrid ; Ecker, Ullrich K. H.
Experimental Psychology. 49 (2002) 2 - p. 120-131 , 2002

Link: https://doi.org/10.1027/..

4

SEMANTISCHE ENTWICKLUNGEN IM MITTELGRIECHISCHEN ANHAND AUSG..:

Steiner, Astrid
Byzantion. 59 (1989) - p. 244-257 , 1989

Link: https://www.jstor.org/st..

5

Reassessing the association: Evaluation of a polyalanine de..:

Walton, Isaac S. ; McCann, Emma ; Weber, Astrid...
Journal of Anatomy. , 2024

Link: https://doi.org/10.1111/..

6

Review of Recurrently Mutated Genes in Craniosynostosis Sup..:

Tooze, Rebecca S. ; Calpena, Eduardo ; Weber, Astrid...
Genes. 14 (2023) 3 - p. 615 , 2023

Link: https://doi.org/10.3390/..

7

Pathogenic variants in the paired-related homeobox 1 gene (..:

Tooze, Rebecca S. ; Miller, Kerry A. ; Swagemakers, Sigrid M.A....
Genetics in Medicine. 25 (2023) 9 - p. 100883 , 2023

Link: https://doi.org/10.1016/..

8

Evaluating the performance of a clinical genome sequencing ..:

Hyder, Zerin ; Calpena, Eduardo ; Pei, Yang...
Genetics in Medicine. 23 (2021) 12 - p. 2360-2368 , 2021

Link: https://doi.org/10.1038/..

9

A genome-wide association study implicates the BMP7 locus a..:

Justice, Cristina M. ; The National Birth Defects Prevention Study ; Cuellar, Araceli...
Human Genetics. 139 (2020) 8 - p. 1077-1090 , 2020

Link: https://doi.org/10.1007/..

10

SMAD6 variants in craniosynostosis: genotype and phenotype ..:

Calpena, Eduardo ; Cuellar, Araceli ; Bala, Krithi...
Genetics in Medicine. 22 (2020) 9 - p. 1498-1506 , 2020

Link: https://doi.org/10.1038/..

11

Correction: SMAD6 variants in craniosynostosis: genotype an..:

Calpena, Eduardo ; Cuellar, Araceli ; Bala, Krithi...
Genetics in Medicine. 22 (2020) 9 - p. 1567 , 2020

Link: https://doi.org/10.1038/..

12

Delineation of dominant and recessive forms of LZTR1‐associ..:

Pagnamenta, Alistair T. ; Kaisaki, Pamela J. ; Bennett, Fenella...
Clinical Genetics. 95 (2019) 6 - p. 693-703 , 2019

Link: https://doi.org/10.1111/..

13

Refining the phenotype associated with GNB1 mutations: Clin..:

Hemati, Parisa ; Revah‐Politi, Anya ; Bassan, Haim...
American Journal of Medical Genetics Part A. 176 (2018) 11 - p. 2259-2275 , 2018

Link: https://doi.org/10.1002/..

14

SET de novo frameshift variants associated with development..:

DDD Study ; Richardson, Ruth ; Splitt, Miranda...
European Journal of Human Genetics. 26 (2018) 9 - p. 1306-1311 , 2018

Link: https://doi.org/10.1038/..

15

A biallelic mutation in IL6ST encoding the GP130 co-recepto..:

Schwerd, Tobias ; Twigg, Stephen R.F. ; Aschenbrenner, Dominik...
Journal of Experimental Medicine. 214 (2017) 9 - p. 2547-2562 , 2017

Link: https://doi.org/10.1084/..