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The American Journal of Human Genetics / A specific CNOT1 m..:

Hattersley, Andrew T ; Barroso, Inês ; De Franco, Elisa...
vignette : https://repositorium.meduniwien.ac.at/titlepage/urn/urn:nbn:at:at-ubmuw:3-34916/128. , 2019

Link: https://resolver.obvsg.at/urn:nbn:at:at-ubmuw:3-34916

RT Journal
T1 <Title>The American Journal of Human Genetics / A specific CNOT1 mutation results in a novel syndrome of pancreatic agenesis and holoprosencephaly through impaired pancreatic and neurological development</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftmeduniwien:oai:repositorium.meduniwien.ac.at_:5751134&Exemplar=1&LAN=DE
				
A1 Hattersley, Andrew T
A1 Barroso, Inês
A1 De Franco, Elisa
A1 Watson, Rachel A
A1 Weninger, Wolfgang Johann
A1 Wong, Chi C
A1 Flanagan, Sarah E
A1 Caswell, Richard
A1 Green, Angela
A1 Tudor, Catherine
A1 Lelliott, Christopher J
A1 Geyer, Stefan H
A1 Maurer-Gesek, Barbara
A1 Reissig, Lukas F
A1 Lango Allen, Hana
A1 Caliebe, Almuth
A1 Siebert, Reiner
A1 Holterhus, Paul Martin
A1 Deeb, Asma
A1 Prin, Fabrice
A1 Hilbrands, Robert
A1 Heimberg, Harry
A1 Ellard, Sian
PB Elsevier
YR 2019
K1 neonatal
K1 diabetes
K1 pancreas
K1 agenesis
K1 genetics
K1 mutation
K1 development
K1 neurological
JF vignette : https://repositorium.meduniwien.ac.at/titlepage/urn/urn:nbn:at:at-ubmuw:3-34916/128
LK http://dx.doi.org/https://resolver.obvsg.at/urn:nbn:at:at-ubmuw:3-34916
DO https://resolver.obvsg.at/urn:nbn:at:at-ubmuw:3-34916
SF ELIB - SuUB Bremen

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