(Q45420913)

English

Autozygosity mapping of a large consanguineous Pakistani family reveals a novel non-syndromic autosomal recessive mental retardation locus on 11p15-tel

scientific article

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 December 2017

Autozygosity mapping of a large consanguineous Pakistani family reveals a novel non-syndromic autosomal recessive mental retardation locus on 11p15-tel (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 December 2017

1 reference

based on heuristic

inferred from title

7

1 reference

Europe PubMed Central

PubMed publication ID

14 December 2017

2

object named as

Shahid Mahmood Baig

1 reference

Europe PubMed Central

PubMed publication ID

14 December 2017

Shoaib Ur Rehman

1

object named as

Shoaib ur Rehman

1 reference

Europe PubMed Central

PubMed publication ID

14 December 2017

author name string

Hans Eiberg

3

1 reference

Europe PubMed Central

PubMed publication ID

14 December 2017

Sijad ur Rehman

4

1 reference

Europe PubMed Central

PubMed publication ID

14 December 2017

Ilyas Ahmad

5

1 reference

Europe PubMed Central

PubMed publication ID

14 December 2017

Naveed Altaf Malik

6

1 reference

Europe PubMed Central

PubMed publication ID

14 December 2017

Lars Hansen

8

1 reference

Europe PubMed Central

PubMed publication ID

14 December 2017

publication date

4 June 2011

1 reference

Europe PubMed Central

PubMed publication ID

14 December 2017

1 reference

Europe PubMed Central

PubMed publication ID

14 December 2017

12

1 reference

Europe PubMed Central

PubMed publication ID

14 December 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

14 December 2017

247-251

1 reference

Europe PubMed Central

PubMed publication ID

14 December 2017

Genetics of Early Onset Cognitive Impairment

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0286-5

21 January 2018

Molecular and comparative genetics of mental retardation

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0286-5

21 January 2018

Truncating neurotrypsin mutation in autosomal recessive nonsyndromic mental retardation

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0286-5

21 January 2018

A gene for nonsyndromic mental retardation maps to chromosome 3p25-pter

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0286-5

21 January 2018

A mutation in a novel ATP-dependent Lon protease gene in a kindred with mild mental retardation

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0286-5

21 January 2018

The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardation

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0286-5

21 January 2018

A new locus for autosomal recessive non-syndromic mental retardation maps to 1p21.1-p13.3.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0286-5

21 January 2018

Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0286-5

21 January 2018

A defect in the ionotropic glutamate receptor 6 gene (GRIK2) is associated with autosomal recessive mental retardation

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0286-5

21 January 2018

Oligosaccharyltransferase-subunit mutations in nonsyndromic mental retardation

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0286-5

21 January 2018

A defect in the TUSC3 gene is associated with autosomal recessive mental retardation

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0286-5

21 January 2018

A truncating mutation of TRAPPC9 is associated with autosomal-recessive intellectual disability and postnatal microcephaly

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0286-5

21 January 2018

Combination of linkage mapping and microarray-expression analysis identifies NF-kappaB signaling defect as a cause of autosomal-recessive mental retardation

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0286-5

21 January 2018

Identification of mutations in TRAPPC9, which encodes the NIK- and IKK-beta-binding protein, in nonsyndromic autosomal-recessive mental retardation

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0286-5

21 January 2018

Mapping of three novel loci for non-syndromic autosomal recessive mental retardation (NS-ARMR) in consanguineous families from Pakistan

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0286-5

21 January 2018

Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0286-5

21 January 2018

Autosomal recessive mental retardation: homozygosity mapping identifies 27 single linkage intervals, at least 14 novel loci and several mutation hotspots.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-011-0286-5

21 January 2018

A computer program for linkage analysis of general human pedigrees

1 reference

https://pubmed.ncbi.nlm.nih.gov/21643797

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mutation in the FOXE3 gene causes congenital primary aphakia in an autosomal recessive consanguineous Pakistani family

1 reference

https://pubmed.ncbi.nlm.nih.gov/21643797

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primer3 on the WWW for general users and for biologist programmers

1 reference

https://pubmed.ncbi.nlm.nih.gov/21643797

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10048-011-0286-5

1 reference

Europe PubMed Central

PubMed publication ID

14 December 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 December 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q45420913&oldid=2207257198"