(Q68296917)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1673297%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

title

Gene localization in a family with X-linked syndromal mental retardation (Prieto syndrome) (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1673297%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

1 reference

A. Watty

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1673297

25 October 2022

F. Prieto

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1673297

25 October 2022

M. Beneyto

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1673297

25 October 2022

M. Neugebauer

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1673297

25 October 2022

A. Gal

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1673297

25 October 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=1673297

25 October 2022

publication date

1 February 1991

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1673297%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

23 September 2019

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fajmg.1320380213

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320380213

https://onlinelibrary.wiley.com/doi/full/10.1002/ajmg.1320380213

25 October 2022

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320380213

American Journal of Medical Genetics Part A

25 October 2022

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1673297%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

volume

38

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1673297%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

issue

2-3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1673297%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

page(s)

234-239

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1673297%20AND%20SRC:MED&resulttype=core&format=json

Linkage analysis suggests at least two loci for X-linked non-specific mental retardation.

23 September 2019

cites work

1

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320380213

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

25 October 2022

4

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320380213

Norrie disease resulting from a gene deletion: clinical features and DNA studies

25 October 2022

5

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320380213

Cytogenetics and Cell Genetics

25 October 2022

6

40

633

Gal

1985

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320380213

X-linked dominant Charcot-Marie-Tooth disease: suggestion of linkage with a cloned DNA sequence from the proximal Xq.

25 October 2022

7

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320380213

Submicroscopic interstitial deletion of the X chromosome explains a complex genetic syndrome dominated by Norrie disease

25 October 2022

8

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320380213

25 October 2022

9

34

397

Glass

1988

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320380213

Probable localisation of the Coffin-Lowry locus in Xp22.2-p22.1 by multipoint linkage analysis.

25 October 2022

10

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320380213

Report of the committee on human gene mapping by recombinant DNA techniques

25 October 2022

11

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320380213

Linkage localization of Börjeson-Forssman-Lehmann syndrome.

25 October 2022

12

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320380213

Börjeson-Forssman-Lehmann syndrome localization

25 October 2022

13

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320380213

X-linked mental retardation with dystonic movements of the hands

25 October 2022

17

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320380213

X-linked dysmorphic syndrome with mental retardation.

25 October 2022

18

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320380213

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

25 October 2022

20

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320380213

A non-syndromal form of X-linked mental retardation (XLMR) is linked to DXS14.

25 October 2022

21

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320380213

Börjeson-Forssman-Lehmann syndrome: clinical manifestations and gene localization to Xq26-27.

25 October 2022

22

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320380213

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

25 October 2022

23

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320380213

Close linkage of the Wieacker-Wolff syndrome to the DNA segment DXYS1 in proximal Xq.

25 October 2022

24

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320380213

Microdeletion in the X-chromosome and prenatal diagnosis in a family with Norrie disease

25 October 2022

25

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320380213

25 October 2022

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1673297%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

1 reference