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Spina Bifida: Genes, Brain, and Development
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title
Spina Bifida: Genes, Brain, and Development
(English)
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main subject
spina bifida
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inferred from title
author
David J. Francis
object named as
David J. Francis
series ordinal
11
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Marcia Barnes
series ordinal
4
object named as
Marcia A. Barnes
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Susan H Landry
series ordinal
6
object named as
Susan H. Landry
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Jack M. Fletcher
series ordinal
1
object named as
Jack M. Fletcher
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Maureen Dennis
series ordinal
2
object named as
Maureen Dennis
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author name string
Hope Northrup
series ordinal
3
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H.Julia Hannay
series ordinal
5
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Kim Copeland
series ordinal
7
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Susan E. Blaser
series ordinal
8
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Larry A. Kramer
series ordinal
9
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Michael E. Brandt
series ordinal
10
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publication date
2004
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published in
International Review of Research in Mental Retardation
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page(s)
63-117
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cites work
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Reading and writing skills in young adults with spina bifida and hydrocephalus
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5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: a HuGE review
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Spina bifida outcome: a 25-year prospective
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Math and numeracy in young adults with spina bifida and hydrocephalus
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The intelligence of hydrocephalic children.
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The content of narrative discourse in children and adolescents after early-onset hydrocephalus and in normally developing age peers
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Regional brain tissue composition in children with hydrocephalus. Relationships with cognitive development.
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Behavioral adjustment of children with hydrocephalus: relationships with etiology, neurological, and family status
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Attentional skills and executive functions in children with early hydrocephalus
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Interaction between undulated and Patch leads to an extreme form of spina bifida in double-mutant mice.
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Functional outcome in young adults with spina bifida and hydrocephalus.
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PAX genes and human neural tube defects: an amino acid substitution in PAX1 in a patient with spina bifida
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Mouse models for neural tube closure defects
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Differential role for the striatum and cerebellum in response to novel movements using a motor learning paradigm.
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Continuing concepts in the management of spina bifida
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Genetic mapping of the human homologue (T) of mouse T(Brachyury) and a search for allele association between human T and spina bifida
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https://api.crossref.org/works/10.1016%2FS0074-7750%2804%2929003-6
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Neural tube closure in humans initiates at multiple sites: evidence from human embryos and implications for the pathogenesis of neural tube defects
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Spina bifida and other neural tube defects
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The two sites of fusion of the neural folds and the two neuropores in the human embryo.
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Cortical axon trajectories and growth cone morphologies in fetuses of acallosal mouse strains
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Dichotic listening in patients with splenial and nonsplenial callosal lesions
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Neural systems control of spatial orienting
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The anterior commissure in man: Functional variation in a multisensory system
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Multi-site neural tube closure in humans and maternal folate supplementation
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A population-based case-control study of anencephalus and spina bifida in a low-risk area
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https://api.crossref.org/works/10.1016%2FS0074-7750%2804%2929003-6
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Dichotic listening in patients with partial section of the corpus callosum
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Pax: genes for mice and men.
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Evidence for multi-site closure of the neural tube in humans
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The splotch-delayed (Spd) mouse mutant carries a point mutation within the paired box of the Pax-3 gene
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Examinations of methylenetetrahydrofolate reductase C677T and A1298C mutations--and in utero viability
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https://api.crossref.org/works/10.1016%2FS0074-7750%2804%2929003-6
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7 January 2021
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Testing for genetic associations with the PAX gene family in a spina bifida population
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https://api.crossref.org/works/10.1016%2FS0074-7750%2804%2929003-6
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Testing for genetic associations in a spina bifida population: analysis of the HOX gene family and human candidate gene regions implicated by mouse models of neural tube defects
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https://api.crossref.org/works/10.1016%2FS0074-7750%2804%2929003-6
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Methylenetetrahydrofolate reductase and spina bifida: evaluation of level of defect and maternal genotypic risk in Hispanics
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https://api.crossref.org/works/10.1016%2FS0074-7750%2804%2929003-6
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Socioeconomic inequalities in risk of congenital anomaly
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https://api.crossref.org/works/10.1016%2FS0074-7750%2804%2929003-6
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Neuropsychological Functioning in Children With Spina Bifida and/or Hydrocephalus
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https://api.crossref.org/works/10.1016%2FS0074-7750%2804%2929003-6
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7 January 2021
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Verbal learning and memory in children with myelomeningocele.
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https://api.crossref.org/works/10.1016%2FS0074-7750%2804%2929003-6
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Topography of the human corpus callosum
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Attention processes in children with shunted hydrocephalus versus attention deficit-hyperactivity disorder
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https://api.crossref.org/works/10.1016%2FS0074-7750%2804%2929003-6
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7 January 2021
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Memory functions in children with early hydrocephalus.
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https://api.crossref.org/works/10.1016%2FS0074-7750%2804%2929003-6
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10.1016/S0074-7750(04)29003-6
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