E-LIB Suche - Ergebnisse für: Ropers, Roland R.

1

Liebe - Urquelle des Kosmos

ein Gespräch über Naturwissenschaft und Religion Herder-Spektrum ; 5965

Dürr, Hans-Peter ; Panikkar, Raimon. - Originalausg. . , 2008

Exemplar: Zentrale:E03 a rel 070/835

2

Wohin geht der Mensch?:

Enomiya-Lassalle, Hugo M. ; Ropers, Roland R. ; Weizsäcker, Carl Friedrich von - 2., erw. Aufl . , 1988

Exemplar: Zentrale:E03 a rel 172/701

3

Zen und christliche Spiritualität:

Enomiya-Lassalle, Hugo M. ; Ropers, Roland R. ; Snela, Bogdan , 1987

Exemplar: Zentrale:E03 a rel 865 f/196

4

Stable long-term outcomes after cochlear implantation in su..:

Fehrmann, M. L. A. ; Huinck, W. J. ; Thijssen, M. E. G....
Journal of Otolaryngology - Head & Neck Surgery. 52 (2023) 1 - p. , 2023

Link: https://doi.org/10.1186/..

5

PLS3 missense variants affecting the actin-binding domains ..:

Petit, Florence ; Longoni, Mauro ; Wells, Julie...
The American Journal of Human Genetics. 110 (2023) 10 - p. 1787-1803 , 2023

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

6

Exploring the missing heritability in subjects with hearing..:

Smits, Jeroen J. ; de Bruijn, Suzanne E. ; Lanting, Cornelis P....
Human Genetics. 141 (2021) 3-4 - p. 465-484 , 2021

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

7

Correction to: Exploring the missing heritability in subjec..:

Smits, Jeroen J. ; de Bruijn, Suzanne E. ; Lanting, Cornelis P....
Human Genetics. , 2021

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

8

Mutations of the aminoacyl-tRNA-synthetases SARS and WARS2 ..:

Musante, Luciana ; Püttmann, Lucia ; Kahrizi, Kimia...
Human Mutation. 38 (2017) 6 - p. 621-636 , 2017

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

9

BOD1 Is Required for Cognitive Function in Humans and Droso..:

Esmaeeli-Nieh, Sahar ; Fenckova, Michaela ; Porter, Iain M....
PLOS Genetics. 12 (2016) 5 - p. e1006022 , 2016

Link: https://doi.org/10.1371/..

10

De novo truncating mutations in ASXL3 are associated with a..:

Bainbridge, Matthew N ; Hu, Hao ; Muzny, Donna M...
Genome Medicine. 5 (2013) 2 - p. 11 , 2013

Link: https://doi.org/10.1186/..

11

Screening Chromosomal Aberrations by Array Comparative Geno..:

Thorwarth, A. ; Mueller, I. ; Biebermann, H....
The Journal of Clinical Endocrinology & Metabolism. 95 (2010) 7 - p. 3446-3452 , 2010

Link: https://doi.org/10.1210/..

12

Recurrent deletion of ZNF630 at Xp11.23 is not associated w..:

Lugtenberg, Dorien ; Zangrande‐Vieira, Luiz ; Kirchhoff, Maria...
American Journal of Medical Genetics Part A. 152A (2010) 3 - p. 638-645 , 2010

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

13

Hypergonadotropic hypogonadism in a patient with inv ins (2..:

Tzschach, A. ; Ramel, C. ; Kron, A....
International Journal of Andrology. 32 (2009) 3 - p. 226-230 , 2009

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

14

Fine mapping of a de novo interstitial 10q22–q23 duplicatio..:

Erdogan, F. ; Belloso, J.M. ; Gabau, E....
European Journal of Medical Genetics. 51 (2008) 1 - p. 81-86 , 2008

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

15

P.1.30 A genomewide duplication- and deletion analysis on p..:

Selch, S. ; Lesch, K.P. ; Romanos, M....
European Neuropsychopharmacology. 17 (2007) - p. S26-S27 , 2007

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