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Functional genomics analysis identifies loss of HNF1B funct..:

Thomson, Ella ; Tran, Minh ; Robevska, Gorjana...
Ella Thomson, Minh Tran, Gorjana Robevska, Katie Ayers, Jocelyn van der Bergen, Prarthna Gopalakrishnan Bhaskaran, Eric Haan, Silvia Cereghini, Alla Vash-Margita, Miranda Margetts, Alison Hensley, Quan Nguyen, Andrew Sinclair, Peter Koopman, Emanuele Pelosi, Functional genomics analysis identifies loss of HNF1B function as a cause of Mayer–Rokitansky–Küster–Hauser syndrome, Human Molecular Genetics, 2022;, ddac262, https://doi.org/10.1093/hmg/ddac262. , 2022

Link: https://scholarworks.montana.edu/xmlui/handle/1/17694

RT Journal
T1 <Title>Functional genomics analysis identifies loss of HNF1B function as a cause of Mayer–Rokitansky–Küster–Hauser syndrome</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftmontanastateu:oai:scholarworks.montana.edu:1_17694&Exemplar=1&LAN=DE
				
A1 Thomson, Ella
A1 Tran, Minh
A1 Robevska, Gorjana
A1 Ayers, Katie
A1 van der Bergen, Jocelyn
A1 Bhaskaran, Prarthna Gopalakrishnan
A1 Haan, Peter
A1 Cereghini, Silvia
A1 Vash-Margita, Alla
A1 Margetts, Miranda
A1 Hensley, Alison
A1 Nguyen, Quan
A1 Sinclair, Andrew
A1 Koopman, Peter
A1 Pelosi, Emanuele
PB Oxford University Press
YR 2022
K1 functional genomics
K1 genomics analysis
K1 HNF1B function
K1 Mayer–Rokitansky–Küster–Hauser syndrome
JF Ella Thomson, Minh Tran, Gorjana Robevska, Katie Ayers, Jocelyn van der Bergen, Prarthna Gopalakrishnan Bhaskaran, Eric Haan, Silvia Cereghini, Alla Vash-Margita, Miranda Margetts, Alison Hensley, Quan Nguyen, Andrew Sinclair, Peter Koopman, Emanuele Pelosi, Functional genomics analysis identifies loss of HNF1B function as a cause of Mayer–Rokitansky–Küster–Hauser syndrome, Human Molecular Genetics, 2022;, ddac262, https://doi.org/10.1093/hmg/ddac262
LK http://dx.doi.org/https://scholarworks.montana.edu/xmlui/handle/1/17694
DO https://scholarworks.montana.edu/xmlui/handle/1/17694
SF ELIB - SuUB Bremen

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