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1.
FOSL2 truncating variants in the last exon cause a neurodevelopmental disorder with scalp and enamel defects.
Genet Med
; 24(12): 2475-2486, 2022 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-36197437
2.
Biallelic truncating variants in MAPKAPK5 cause a new developmental disorder involving neurological, cardiac, and facial anomalies combined with synpolydactyly.
Genet Med
; 23(4): 679-688, 2021 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-33442026
3.
Phenotypic and genetic diversity of Moroccan rhizobia isolated from Vicia faba and study of genes that are likely to be involved in their osmotolerance.
Syst Appl Microbiol
; 41(1): 51-61, 2018 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-29198596
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