Neuropathologic research strategies in holoprosencephaly. - Wikidata - wikimedia - TriplyDB

Neuropathologic research strategies in holoprosencephaly.

Neuropathologic research strategies in holoprosencephaly.

http://www.wikidata.org/entity/Q34489252

about

Neuroimaging in spasticity and movement disorders.Neuroimaging in cerebral palsy: Patterns of brain dysgenesis and injury.Differential regulation of the zebrafish orthopedia 1 gene during fate determination of diencephalic neurons.Links between abnormal brain structure and cognition in holoprosencephaly Embryology of the neural crest: its inductive role in the neurocutaneous syndromes.Semilobar Holoprosencephaly with Neurogenic Hypernatraemia: Two new cases.Wiring Olfaction: The Cellular and Molecular Mechanisms that Guide the Development of Synaptic Connections from the Nose to the Cortex.A novel role for zebrafish zic2a during forebrain development.Perfil de habilidades do desenvolvimento em crianças com holoprosencefalia e holoprosencefalia like

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P2860

Neuropathologic research strategies in holoprosencephaly.

http://www.wikidata.org/entity/Q34489252

description

2001 nî lūn-bûn

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2001 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2001 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2001年の論文

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2001年論文

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2001年論文

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2001年論文

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2001年論文

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2001年論文

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2001年论文

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Neuropathologic research strategies in holoprosencephaly.

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Neuropathologic research strategies in holoprosencephaly.

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Neuropathologic research strategies in holoprosencephaly.

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Neuropathologic research strategies in holoprosencephaly.

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Neuropathologic research strategies in holoprosencephaly.

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Neuropathologic research strategies in holoprosencephaly.

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Neuropathologic research strategies in holoprosencephaly.

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088307380101601211

P1433

Journal of Child Neurology

P1476

Neuropathologic research strategies in holoprosencephaly.

@en

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H B Sarnat

http://www.w3.org/2001/XMLSchema#string

L Flores-Sarnat

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P2860

Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse

Expression of a large family of POU-domain regulatory genes in mammalian brain development

Progressive impairment of developing neuroendocrine cell lineages in the hypothalamus of mice lacking the Orthopedia gene

Development and survival of the endocrine hypothalamus and posterior pituitary gland requires the neuronal POU domain factor Brn-2

Role of the Bicoid-related homeodomain factor Pitx1 in specifying hindlimb morphogenesis and pituitary development

Malformations of cortical development and epilepsy.

Identification, chromosomal assignment, and expression analysis of the human homeodomain-containing gene Orthopedia (OTP).

Diverse migratory pathways in the developing cerebral cortex.

Chemically defined neuron groups and their subpopulations in the glomerular layer of the rat main olfactory bulb: III. Structural features of calbindin D28K-immunoreactive neurons.

Towards a greater understanding of the pathogenesis of holoprosencephaly.

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scholarly article

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holoprosencephaly