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Biorxiv : the Preprint Server for Biology
|
September 5, 2025
Teneurin-3 and latrophilin-2 are required for somatotopic map formation and somatosensory topognosis
Kevin T Sangster, Xinying Zhang, Daniel Del Toro, et al.
Journal of Neuropathology and Experimental Neurology
|
January 16, 2014
Cytomegalovirus-induced brain malformations in fetuses
Natacha Teissier, Catherine Fallet-Bianco, Anne-Lise Delezoide, et al.
The Journal of Comparative Neurology
|
November 18, 2006
Magnetic resonance imaging and histological studies of corpus callosal and hippocampal abnormalities linked to doublecortin deficiency
Caroline Kappeler, Marc Dhenain, Françoise Phan Dinh Tuy, et al.
American Journal of Medical Genetics. Part A
|
January 18, 2019
Homozygous/compound heterozygote RYR1 gene variants: Expanding the clinical spectrum
Ebba Alkhunaizi, Shirley Shuster, Patrick Shannon, et al.
Journal of Medical Genetics
|
February 5, 2015
Disruption of CLPB is associated with congenital microcephaly, severe encephalopathy and 3-methylglutaconic aciduria
José-Mario Capo-Chichi, Sarah Boissel, Edna Brustein, et al.
Human Molecular Genetics
|
September 11, 2010
Mutations in the neuronal ß-tubulin subunit TUBB3 result in malformation of cortical development and neuronal migration defects
Karine Poirier, Yoann Saillour, Nadia Bahi-Buisson, et al.
American Journal of Medical Genetics. Part A
|
January 20, 2007
Matthew-Wood syndrome: report of two new cases supporting autosomal recessive inheritance and exclusion of FGF10 and FGFR2
Jelena Martinovic-Bouriel, Céline Bernabé-Dupont, Christelle Golzio, et al.
American Journal of Medical Genetics. Part A
|
December 4, 2019
Second report of RING finger protein 113A (RNF113A) involvement in a Mendelian disorder
Marine Tessarech, Magali Gorce, Françoise Boussion, et al.
Brain : a Journal of Neurology
|
October 9, 2010
GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex
Nadia Bahi-Buisson, Karine Poirier, Nathalie Boddaert, et al.
American Journal of Human Genetics
|
March 9, 2010
Mutations in FLVCR2 are associated with proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome (Fowler syndrome)
Esther Meyer, Christopher Ricketts, Neil V Morgan, et al.
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Search research articles
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Showing results (41-50 of 64) with videos related to
Sort By:
Page
of 7
Biorxiv : the Preprint Server for Biology
|
September 5, 2025
Teneurin-3 and latrophilin-2 are required for somatotopic map formation and somatosensory topognosis
Kevin T Sangster, Xinying Zhang, Daniel Del Toro, et al.
Journal of Neuropathology and Experimental Neurology
|
January 16, 2014
Cytomegalovirus-induced brain malformations in fetuses
Natacha Teissier, Catherine Fallet-Bianco, Anne-Lise Delezoide, et al.
The Journal of Comparative Neurology
|
November 18, 2006
Magnetic resonance imaging and histological studies of corpus callosal and hippocampal abnormalities linked to doublecortin deficiency
Caroline Kappeler, Marc Dhenain, Françoise Phan Dinh Tuy, et al.
American Journal of Medical Genetics. Part A
|
January 18, 2019
Homozygous/compound heterozygote RYR1 gene variants: Expanding the clinical spectrum
Ebba Alkhunaizi, Shirley Shuster, Patrick Shannon, et al.
Journal of Medical Genetics
|
February 5, 2015
Disruption of CLPB is associated with congenital microcephaly, severe encephalopathy and 3-methylglutaconic aciduria
José-Mario Capo-Chichi, Sarah Boissel, Edna Brustein, et al.
Human Molecular Genetics
|
September 11, 2010
Mutations in the neuronal ß-tubulin subunit TUBB3 result in malformation of cortical development and neuronal migration defects
Karine Poirier, Yoann Saillour, Nadia Bahi-Buisson, et al.
American Journal of Medical Genetics. Part A
|
January 20, 2007
Matthew-Wood syndrome: report of two new cases supporting autosomal recessive inheritance and exclusion of FGF10 and FGFR2
Jelena Martinovic-Bouriel, Céline Bernabé-Dupont, Christelle Golzio, et al.
American Journal of Medical Genetics. Part A
|
December 4, 2019
Second report of RING finger protein 113A (RNF113A) involvement in a Mendelian disorder
Marine Tessarech, Magali Gorce, Françoise Boussion, et al.
Brain : a Journal of Neurology
|
October 9, 2010
GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex
Nadia Bahi-Buisson, Karine Poirier, Nathalie Boddaert, et al.
American Journal of Human Genetics
|
March 9, 2010
Mutations in FLVCR2 are associated with proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome (Fowler syndrome)
Esther Meyer, Christopher Ricketts, Neil V Morgan, et al.
Page
of 7