(Q40403187)

20 September 2017

title

Diagnostic yield of the neurologic assessment of the developmentally delayed child (English)

1 reference

20 September 2017

Majnemer A

1

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20 September 2017

Shevell MI

series ordinal

2

1 reference

20 September 2017

language of work or name

English

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publication date

1 August 1995

1 reference

The Journal of Pediatrics

20 September 2017

published in

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20 September 2017

volume

127

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20 September 2017

issue

2

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20 September 2017

page(s)

193-199

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Pediatric assessment of the child with developmental delay.

20 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2895%2970294-6

Evaluation of the Child with Idiopathic Mental Retardation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2895%2970294-6

The biological origin of mild mental retardation. A critical review

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2895%2970294-6

The infant or young child with developmental delay

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2895%2970294-6

A study of institutionalized mentally retarded patients in Manitoba. I: Classification and preventability.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2895%2970294-6

Epidemiology of mental retardation--a Swedish survey.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2895%2970294-6

Influence of demographic factors on annual Down's syndrome births in Ohio, 1970-1979, and the United States, 1920-1979

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2895%2970294-6

Intrapartum asphyxia: A rare cause of cerebral palsy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2895%2970294-6

Use of the CT scan in the medical evaluation of the mentally retarded child

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2895%2970294-6

Value of computerised tomography in children with non-specific mental subnormally

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2895%2970294-6

Computed tomography in non-specific mental retardation and idiopathic epilepsy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2895%2970294-6

Wide cavum septum pellucidum: a marker of disturbed brain development

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2895%2970294-6

Macro cisterna magna: a marker for maldevelopment of the brain?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2895%2970294-6

Clinical and morphometric analysis of the hypoplastic corpus callosum

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2895%2970294-6

Old syndromes and new cytogenetics.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2895%2970294-6

Identification of the origin of centromeres in whole-arm translocations using fluorescent in situ hybridization with alpha-satellite DNA probes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2895%2970294-6

Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2895%2970294-6

Metabolic Abnormalities Detected in a Survey of Mentally Backward Individuals in Northern Ireland

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2895%2970294-6

Inborn errors of metabolism: the essentials of clinical diagnosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2895%2970294-6

Phenotypic and genotypic variability of generalized peroxisomal disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2895%2970294-6

Agenesis of the corpus callosum: a marker for inherited metabolic disease?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2895%2970294-6

Cerebral dysgenesis and lactic acidemia: an MRI/MRS phenotype associated with pyruvate dehydrogenase deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2895%2970294-6

Molecular genetic advances in fragile X syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2895%2970294-6

Predictive value of screening for different areas of development

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2895%2970294-6

inferred from DOI database lookup

7 January 2021

based on heuristic

Assessment and management of the developmentally delayed infant in primary care.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2895%2970294-6

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0022-3476(95)70294-6

1 reference

20 September 2017

1 reference