Hoeber, Jan
47  Ergebnisse:
Personensuche X
?
2

Monoallelic and bi-allelic variants in NCDN cause neurodeve..:

Fatima, Ambrin ; Hoeber, Jan ; Schuster, Jens...
The American Journal of Human Genetics.  109 (2022)  3 - p. 542-546 , 2022
 
?
7

ZEB2 haploinsufficient Mowat-Wilson syndrome induced plurip..:

Jens Schuster ; Joakim Klar ; Ayda Khalfallah...
https://www.frontiersin.org/articles/10.3389/fnmol.2022.988993/full.  , 2022
 
?
 
?
 
?
13

Monoallelic and bi-allelic variants in NCDN cause neurodeve..:

Fatima, Ambrin ; Hoeber, Jan ; Schuster, Jens...
The American Journal of Human Genetics.  108 (2021)  4 - p. 739-748 , 2021
 
?
14

Monoallelic and bi-allelic variants in NCDN cause neurodeve..:

Fatima, Ambrin ; Hoeber, Jan ; Schuster, Jens...
American Journal of Human Genetics, 0002-9297, 2021, 108:4, s. 739-748.  , 2021
 
?
15

Mono-allelic and bi-allelic variants in NCDN cause neurodev..:

Fatima, Ambrin ; Hoeber, Jan ; Schuster, Jens...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2021.02.015.  , 2021
 
1-15
Mehr Literatur finden