Laan, Loora
45  Ergebnisse:
Personensuche X
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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
 
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3

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
 
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ZEB2 haploinsufficient Mowat-Wilson syndrome induced plurip..:

Schuster, Jens ; Klar, Joakim ; Khalfallah, Ayda...
Frontiers in Molecular Neuroscience, 1662-5099, 2022, 15,.  , 2022
 
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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
 
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