Results 121 to 130 of about 4,846 (140)

Sciphy: A Bayesian phylogenetic framework using sequential genetic lineage tracing data

Seidel S, Zwaans A, Regalado S, Choi J, Shendure J, Stadler T.   +5 more
europepmc   +1 more source

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Splicing Interruption by Intron Variants in CSNK2B Causes Poirier–Bienvenu Neurodevelopmental Syndrome: A Focus on Genotype–Phenotype Correlations

Frontiers in Neuroscience, 2022
Wen Zhang, Nan Pang, Fei Yin
exaly  

Haploinsufficiency as a Foreground Pathomechanism of Poirer-Bienvenu Syndrome and Novel Insights Underlying the Phenotypic Continuum of CSNK2B-Associated Disorders

Genes, 2023
Mariateresa Di Stazio, Caterina Zanus, Flavio Faletra   +2 more
exaly  

Expanding Phenotype of Poirier–Bienvenu Syndrome: New Evidence from an Italian Multicentrical Cohort of Patients

Genes, 2022
Alessandro Orsini, Andrea Santangelo, Diego Peroni   +2 more
exaly  

Case report: Two cases of Poirier-Bienvenu neurodevelopmental syndrome and review of literature

Frontiers in Pediatrics, 2023
exaly  

Comparing Two Neurodevelopmental Disorders Linked to CK2: Okur-Chung Neurodevelopmental Syndrome and Poirier-Bienvenu Neurodevelopmental Syndrome—Two Sides of the Same Coin?

Frontiers in Molecular Biosciences, 2022
Thierry Bienvenu, Heike Rebholz
exaly  

De Novo CSNK2B Mutations in Five Cases of Poirier–Bienvenu Neurodevelopmental Syndrome

Frontiers in Neurology, 2022
exaly  

Clinical and genetic analysis of six Chinese children with Poirier-Bienvenu neurodevelopmental syndrome caused by CSNK2B mutation

Neurogenetics, 2021
exaly  

Reproductive Development in Oilseed Rape (Brassica napus cv. Bienvenu)

Annals of Botany, 1990
exaly