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1.
De novo variants in DENND5B cause a neurodevelopmental disorder.
Am J Hum Genet
; 111(3): 529-543, 2024 Mar 07.
Article
in English
| MEDLINE | ID: mdl-38387458
2.
Inherited glycosylphosphatidylinositol defects cause the rare Emm-negative blood phenotype and developmental disorders.
Blood
; 137(26): 3660-3669, 2021 07 01.
Article
in English
| MEDLINE | ID: mdl-33763700
3.
Biallelic loss of EMC10 leads to mild to severe intellectual disability.
Ann Clin Transl Neurol
; 9(7): 1080-1089, 2022 07.
Article
in English
| MEDLINE | ID: mdl-35684946
4.
Genotype specific age related changes in a transgenic rat model of Huntington's disease.
Neuroimage
; 58(4): 1006-16, 2011 Oct 15.
Article
in English
| MEDLINE | ID: mdl-21767653
5.
Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder.
Nat Commun
; 12(1): 2558, 2021 05 07.
Article
in English
| MEDLINE | ID: mdl-33963192
6.
Multimodal In Vivo Imaging of Tumorigenesis and Response to Chemotherapy in a Transgenic Mouse Model of Mammary Cancer.
Mol Imaging Biol
; 18(4): 617-26, 2016 08.
Article
in English
| MEDLINE | ID: mdl-26630973
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