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Disorders of neuronal migration
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
3545413
retrieved
14 September 2017
review article
1 reference
stated in
Europe PubMed Central
title
Disorders of neuronal migration.
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
3545413
retrieved
14 September 2017
author name string
Barth PG
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
3545413
retrieved
14 September 2017
publication date
1 February 1987
1 reference
stated in
Europe PubMed Central
PubMed ID
3545413
retrieved
14 September 2017
published in
Canadian Journal of Neurological Sciences
1 reference
stated in
Europe PubMed Central
PubMed ID
3545413
retrieved
14 September 2017
volume
14
1 reference
stated in
Europe PubMed Central
PubMed ID
3545413
retrieved
14 September 2017
page(s)
1-16
1 reference
stated in
Europe PubMed Central
PubMed ID
3545413
retrieved
14 September 2017
issue
1
1 reference
stated in
Europe PubMed Central
PubMed ID
3545413
retrieved
14 September 2017
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7 January 2021
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Immunoperoxidase localization of glial fibrillary acidic protein in radial glial cells and astrocytes of the developing rhesus monkey brain
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7 January 2021
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7 January 2021
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7 January 2021
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LISSENCEPHALY
1 reference
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Crossref
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7 January 2021
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Holoprosencephaly and agenesis of the corpus callosum: frequency of associated malformations
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Evolution of Bergmann glia in developing human fetal cerebellum: a Golgi, electron microscopic and immunofluorescent study
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Crossref
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7 January 2021
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Embryogenesis of the inferior olivary nucleus in the rat: a radioautographic study and a re-evaluation of the rhombic lip.
1 reference
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Crossref
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7 January 2021
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The mechanism of arrest of neuronal migration in the Zellweger malformation: An hypothesis based upon cytoarchitectonic analysis
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Crossref
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Crossref
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7 January 2021
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Peroxisomal and mitochondrial defects in the cerebro-hepato-renal syndrome.
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Crossref
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7 January 2021
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Weaver Mutant Mouse Cerebellum: Defective Neuronal Migration Secondary to Abnormality of Bergmann Glia
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Crossref
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7 January 2021
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Expression of Glial Fibrillary Acidic Protein in Immature Oligodendroglia
1 reference
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Crossref
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7 January 2021
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inferred from DOI database lookup
The cerebro-hepato-renal (Zellweger) syndrome: lamellar lipid profiles in adrenocortical, hepatic mesenchymal, astrocyte cells and increased levels of very long chain fatty acids and phytanic acid in the plasma.
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Crossref
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7 January 2021
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Modulation of Cell Adhesion during Induction, Histogenesis, and Perinatal Development of the Nervous System
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Crossref
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7 January 2021
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Granule cell as a site of gene action in the weaver mouse cerebellum: evidence from heterozygous mutant chimeras.
1 reference
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Crossref
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7 January 2021
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Globoid cells, glial nodules, and peculiar fibrillary changes in the cerebro-hepato-renal syndrome of zellweger
1 reference
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Crossref
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7 January 2021
based on heuristic
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Heterogeneity of congenital retinal non-attachment, falciform folds and retinal dysplasia. A guide to genetic counselling
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Crossref
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7 January 2021
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Cell determination and regulation during development of neuroblasts and neurones in grasshopper embryo
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7 January 2021
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Ventricular diverticula with localized dysgenesis of the temporal lobe in cloverleaf skull anomaly
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Polyamine metabolism and function
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Crossref
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7 January 2021
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Neuropathologic findings in thanatophoric dysplasia
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Crossref
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7 January 2021
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Structural Anomalies in the Cerebellum in Association With Trisomy
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Crossref
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https://api.crossref.org/works/10.1017%2FS031716710002610X
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7 January 2021
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Patterns of cell and fiber distribution in the neocortex of the reeler mutant mouse
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Crossref
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7 January 2021
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Agyria-pachygyria (lissencephaly syndrome)
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Crossref
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https://api.crossref.org/works/10.1017%2FS031716710002610X
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7 January 2021
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The syndrome of absence of the septum pellucidum with porencephalies and other developmental defects.
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Multiple acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two brothers. I. Clinical, metabolical, and biochemical findings.
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based on heuristic
inferred from DOI database lookup
Multiple acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two newborn brothers. II. Morphology and pathogenesis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital muscular dystrophy as a disease of the central nervous system
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A case of arthrogryposis multiplex congenita with lesions in the nervous system
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An autoradiographic analysis of histogenesis in the mouse cerebellum
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neuropathological and Golgi study on a case of thanatophotoric dysplasia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The relationship between prenatal porencephaly and the encephalomalacias of early life.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Zellweger syndrome: subcellular pathology, neuropathology, and the demonstration of pneumocystis carinii pneumonitis in two siblings
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Peroxisomal disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Peroxisomal disorders: a newly recognised group of genetic diseases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Infantile spasms associated with hemihypsarrhythmia and hemimegalencephaly
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Radial glia in the human fetal cerebrum: a combined Golgi, immunofluorescent and electron microscopic study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The cerebrohepatorenal (Zellweger) syndrome. Increased levels and impaired degradation of very-long-chain fatty acids and their use in prenatal diagnosis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Effects of methylmercury on DNA synthesis of human fetal astrocytes: a radioautographic study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lissencephaly
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
[Familial microcephalies due to cerebral malformation. Anatomical and clinical study]
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pachygyria and congenital nephrosis disorder of migration and neuronal orientation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Experimental studies on cerebellar foliation. I. A qualitative morphological analysis of cerebellar fissuration defects after neonatal treatment with 6-OHDA in the rat.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A Golgi study of the brain malformation in Zellweger's cerebro-hepato-renal disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Schizencephalies; a study of the congenital clefts in the cerebral mantle; clefts with fused lips.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Syndromes with lissencephaly. II: Walker-Warburg and cerebro-oculo-muscular syndromes and a new syndrome with type II lissencephaly
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital progressive muscular dystrophy of the Fukuyama type - clinical, genetic and pathological considerations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An autopsy case of hemimegalencephaly
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Defects in specific associations between astroglia and neurons occur in microcultures of weaver mouse cerebellar cells.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Distribution and morphology of corticospinal tract neurons in reeler mouse cortex by the retrograde HRP method.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prenatal clastic encephalopathies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Time of origin or corresponding cell classes in the cerebral cortex of normal and reeler mutant mice: an autoradiographic analysis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transient expression of a surface antigen on a small subset of neurones during embryonic development
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Occipital encephalocele: a pathologic and anatomic analysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hypomelanosis of Ito (incontinentia pigmenti achromians)--a clinicopathologic study: macrocephaly and gray matter heterotopias.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cell recognition during neuronal development.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Malformations of the central nervous system in trisomy 18 syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Brain malformations in the trisomy 18 syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Further comments on the lissencephaly syndromes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Alcohol embryo- and fetopathy. Neuropathology of 3 children and 3 fetuses
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Brain abnormalities in infants with Potter syndrome (oligohydramnios tetrad).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pathological features in the de Lange syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Bilateral encephaloclastic lesions in a 26 week gestation fetus: effect on neuroblast migration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Encephalocraniocutaneous lipomatosis. A new example of ectomesodermal dysgenesis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal recessive eye and brain anomalies: Warburg syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Unilateral megalencephaly, cerebral cortical dysplasia, neuronal hypertrophy, and heterotopia: Cytomorphometric, fluorometric cytochemical, and biochemical analyses
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isotretinoin dysmorphic syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cerebro-hepato-renal syndrome of Zellweger: an inherited disorder of neuronal migration.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Unilateral megalencephaly: hamartoma or neoplasm?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isotretinoin teratogenicity. Case report with neuropathologic findings.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Parabiotic twin syndrome with topical isocortical disruption and gastroschisis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Long-term pathological effects of prenatal x-irradiation on the central nervous system of the rat
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Recognition of the fetal alcohol syndrome in early infancy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Brain malformations related to prenatal exposure to ethanol
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The pathogenesis of brain abnormalities in the fetal alcohol syndrome: an integrating hypothesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Dandy-Walker syndrome. A clinicopathological study based on 28 cases.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Effects of methylmercury on human fetal neurons and astrocytes in vitro: a time-lapse cinematographic, phase and electron microscopic study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Studies on ectopic granule cells in the cerebellar cortex--with a hypothesis as to their aetiology and pathogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Oral-facial-digital syndrome. A case with necropsy findings.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS031716710002610X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1017/S031716710002610X
0 references
PubMed ID
3545413
1 reference
stated in
Europe PubMed Central
PubMed ID
3545413
retrieved
14 September 2017
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