(Q33598273)

28 July 2017

MASA syndrome: new clinical features and linkage analysis using DNA probes (English)

1 reference

28 July 2017

1 reference

Schrander-Stumpel C

1

1 reference

28 July 2017

Legius E

series ordinal

2

1 reference

28 July 2017

Fryns JP

series ordinal

3

1 reference

28 July 2017

Cassiman JJ

series ordinal

4

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 November 1990

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

27

1 reference

28 July 2017

688-692

1 reference

28 July 2017

11

1 reference

Mental retardation-clasped thumb syndrome.

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017259

X-linked mental retardation associated with bilateral clasp thumb anomaly.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017259

The MASA syndrome: a new heritable mental retardation syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017259

X linked hydrocephalus: a survey of a 20 year period in Victoria, Australia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017259

Etiological heterogeneity in X-linked spastic paraplegia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017259

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017259

Linkage studies with the gene for an X-linked syndrome of mental retardation, microcephaly and spastic diplegia (MRX2)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017259

MASA syndrome: further clinical delineation and chromosomal localisation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017259

Aqueductal Stenosis in X-Linked Hydrocephalus: a Secondary Phenomenon?

21 June 2018

1 reference

12 December 2020

X-linked hydrocephalus

1 reference

12 December 2020

A new polymorphic marker very closely linked to DXS52 in the q28 region of the human X chromosome

1 reference

12 December 2020

X-linked spastic paraplegia: evidence for homogeneity with a variable phenotype

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.27.11.688

1 reference

28 July 2017

1 reference

28 July 2017

1 reference