Suchergebnisse - "Guimiot, Fabien"

1

Mowat–Wilson syndrome in a fetus with antenatal diagnosis of short corpus callosum: Advocacy for standard autopsy

von: Spaggiari, Emmanuel

2013transfer abstract, in: Edge minimization in de Bruijn graphs

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2

Identification of a novel brain-specific and reelin-regulated gene that encodes a protein colocalized with synapsin

von: Kuvbachieva, Anelia

2004, in: European journal of neuroscience

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3

Human neuropathology confirms projection neuron and interneuron defects and delayed oligodendrocyte production and maturation in FOXG1 syndrome

von: Wilpert, Nina-Maria

2021transfer abstract, in: Edge minimization in de Bruijn graphs

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4

3D-FISH analysis reveals chromatid cohesion defect during interphase in Roberts syndrome

von: Dupont, Celine

2014, in: Molecular cytogenetics

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5

Hydrocephalus due to multiple ependymal malformations is caused by mutations in the MPDZ gene

von: Saugier-Veber, Pascale

2017, in: Acta Neuropathologica Communications

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6

Safety study of Ciprofloxacin in newborn mice

von: Bourgeois, Thomas

2016transfer abstract, in: In situ DRIFTS investigation for the oxidation of toluene by ozone over Mn/HZSM-5, Ag/HZSM-5 and Mn–Ag/HZSM-5 catalysts

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7

Sostdc1 is expressed in all major compartments of developing and adult mammalian eyes

von: Valensi, Maud

2019, in: Graefe's archive for clinical and experimental ophthalmology

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8

Mutations in tubulin genes are frequent causes of various foetal malformations of cortical development including microlissencephaly

von: Fallet-Bianco, Catherine

2014, in: Acta Neuropathologica Communications

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9

Extracellular LGALS3BP regulates neural progenitor position and relates to human cortical complexity

von: Christina Kyrousi

2021, in: Nature Communications

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10

Evidence of disrupted rhombic lip development in the pathogenesis of Dandy–Walker malformation

von: Haldipur, Parthiv

2021, in: Acta neuropathologica

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