(Q52040978)

20 April 2018

title

Linkage to Xq28 in a family with nonspecific X-linked mental retardation (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1362558

18 September 2022

author name string

A. M. Nordström

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1362558

18 September 2022

M. Penttinen

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1362558

18 September 2022

H. von Koskull

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1362558

18 September 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1362558

18 September 2022

publication date

1 November 1992

1 reference

20 April 2018

published in

Human Genetics

1 reference

20 April 2018

volume

90

1 reference

20 April 2018

issue

3

1 reference

20 April 2018

page(s)

263-266

1 reference

20 April 2018

cites work

XLMR genes: update 1990.

1 reference

12 December 2020

Strategies for multilocus linkage analysis in humans

1 reference

12 December 2020

Four chromosomal breakpoints and four new probes mark out a 10-cM region encompassing the fragile-X locus (FRAXA)

1 reference

12 December 2020

A clinically useful DNA probe closely linked to haemophilia A

1 reference

12 December 2020

Improved DNA markers for efficient analysis of fragile X families

1 reference

12 December 2020

Genetic mapping and diagnosis of haemophilia A achieved through a BclI polymorphism in the factor VIII gene

1 reference

12 December 2020

Physical fine mapping of the choroideremia locus using Xq21 deletions associated with complex syndromes.

1 reference

12 December 2020

MASA syndrome: further clinical delineation and chromosomal localisation

1 reference

12 December 2020

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

1 reference

12 December 2020

The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency

1 reference

12 December 2020

On the gates of hell and a most unusual gene

1 reference

12 December 2020

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

1 reference

12 December 2020

Genetic mapping of new RFLPs at Xq27–q28

1 reference

12 December 2020

Assignment of X-linked hydrocephalus to Xq28 by linkage analysis

1 reference

12 December 2020

Localisation of the MRX3 gene for non-specific X linked mental retardation

1 reference

12 December 2020

Localization of the gene for a syndrome of X-linked skeletal dysplasia and mental retardation to Xq27-qter.

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00220075

1 reference

20 April 2018

1 reference

20 April 2018