Allan-Herndon syndrome. I. Clinical studies (Q35198475)

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28 September 2019

title

Allan-Herndon syndrome. I. Clinical studies (English)

1 reference

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28 September 2019

author name string

Stevenson RE

1

1 reference

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28 September 2019

Goodman HO

2

1 reference

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28 September 2019

Schwartz CE

3

1 reference

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28 September 2019

Simensen RJ

4

1 reference

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28 September 2019

McLean WT Jr

5

1 reference

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28 September 2019

Herndon CN

6

1 reference

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28 September 2019

language of work or name

English

0 references

publication date

1 September 1990

1 reference

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28 September 2019

number of pages

8

1 reference

American Journal of Human Genetics

inferred from page(s)

published in

1 reference

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28 September 2019

volume

47

1 reference

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28 September 2019

issue

3

1 reference

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28 September 2019

page(s)

446-453

1 reference

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A sex-linked recessive form of spastic paraplegia

28 September 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683863

Severely retarded children in a London area: prevalence and provision of services

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683863

The nosology of mental retardation: including the report of a survey of 1378 mentally retarded individuals at the Walter E. Fernald State School

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683863

Infantile X-linked ataxia and deafness: a new clinicopathologic entity?

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683863

Linkage studies of X-linked recessive spastic paraplegia using DNA probes.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683863

MASA syndrome: further clinical delineation and chromosomal localisation

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683863

X-linked olivopontocerebellar atrophy

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683863

X-linked recessive type of pure spastic paraplegia in a large pedigree: absence of detectable linkage with Xg

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683863

Recurrence risks in families of children with symmetrical spasticity

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683863

A new X-linked syndrome with muscle atrophy, congenital contractures, and oculomotor apraxia

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683863

Sex-linked spastic paraplegia

26 September 2018

1 reference

12 December 2020

Two kindreds with a sex-linked recessive form of spastic paraplegia

1 reference

12 December 2020

Heterogeneity of X-linked recessive (spino)cerebellar ataxia with or without spastic diplegia

1 reference

12 December 2020

Unusual form of cerebellar ataxia with sex-linked inheritance

1 reference

12 December 2020

Identifiers

1 reference

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28 September 2019

1 reference