(Q35195848)

7 August 2017

Localization of DNA sequences to a region within Xp11.21 between incontinentia pigmenti (IP1) X-chromosomal translocation breakpoints (English)

1 reference

7 August 2017

J L Gorski

1

1 reference

7 August 2017

E N Burright

2

1 reference

7 August 2017

C E Harnden

3

1 reference

7 August 2017

C K Stein

4

1 reference

7 August 2017

T W Glover

5

1 reference

7 August 2017

E L Reyner

6

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 January 1991

1 reference

American Journal of Human Genetics

7 August 2017

1 reference

7 August 2017

48

1 reference

7 August 2017

53-64

1 reference

7 August 2017

1

1 reference

Deletion and amplification of the HGPRT locus in Chinese hamster cells

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

Regional localization on the human X of DNA segments cloned from flow sorted chromosomes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

Two cases of X/autosome translocation in females with incontinentia pigmenti.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

Rapid transfer of DNA from agarose gels to nylon membranes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

Incontinentia pigmenti (IP) and r(X). Tentative mapping of the IP locus to the X juxtacentromeric region.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

The sex-determining region of the human Y chromosome encodes a finger protein.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

Molecular analysis of a constitutional X-autosome translocation in a female with muscular dystrophy.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

Separation of large DNA molecules by contour-clamped homogeneous electric fields

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

Regional mapping panel for human chromosome 17: application to neurofibromatosis type 1.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

Cosmid vectors for rapid genomic walking, restriction mapping, and gene transfer

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

Identification of the cystic fibrosis gene: chromosome walking and jumping

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

Evidence for genetic heterogeneity in tuberous sclerosis

28 July 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

28 July 2018

12 December 2020

The gene for incontinentia pigmenti is assigned to Xq28.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

Report of the committee on the genetic constitution of the X chromosome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

Linkage heterogeneity between X-linked retinitis pigmentosa and a map of 10 RFLP loci

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

Yeast artificial chromosomes with 200- to 800-kilobase inserts of human DNA containing HLA, V kappa, 5S, and Xq24-Xq28 sequences.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

Segregation of the Huntington disease region of human chromosome 4 in a somatic cell hybrid

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

Physical mapping of the von Recklinghausen neurofibromatosis region on chromosome 17.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

Reverse genetics and human disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

Pigmentary abnormalities and mosaicism for chromosomal aberration: association with clinical features similar to hypomelanosis of Ito.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

Mapping of a gene determining tuberous sclerosis to human chromosome 11q14-11q23.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

Incontinentia pigmenti. A world statistical analysis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

X-linked dominant inherited diseases with lethality in hemizygous males

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682742

Incontinentia pigmenti and X-autosome translocations. Non-isotopic in situ hybridization with an X-centromere-specific probe (pSV2X5) reveals a possible X-centromeric breakpoint in one of five published cases

26 September 2018

1 reference

12 December 2020

Incontinentia pigmenti: Xp breakpoint is not the same in a case of r(X) and in X/autosome translocations

1 reference

12 December 2020

A somatic cell hybrid panel to facilitate identification of DNA sequences in the vicinity of the incontinentia pigmenti locus (IP1)

1 reference

12 December 2020

Molecular genetics. A gene for Wilms tumour?

1 reference

12 December 2020

A method for generating hybrids containing nonselected fragments of human chromosomes

1 reference

12 December 2020

Translocation (X;9)(p11;q34) in a girl with incontinentia pigmenti (IP): implications for the regional assignment of the IP locus to Xp11?

1 reference

12 December 2020

Translocation (X;13)(p11.21;q12.3) in a girl with incontinentia pigmenti and bilateral retinoblastoma

1 reference

12 December 2020

Molecular heterogeneity of translocations associated with muscular dystrophy

1 reference

12 December 2020

Gene for incontinentia pigmenti maps to band Xp11 with an (X;10) (p11;q22) translocation

1 reference

12 December 2020

Isolation of genomic DNA

1 reference

12 December 2020

A second genetic locus for autosomal dominant polycystic kidney disease

1 reference

12 December 2020

A primary genetic map of the pericentromeric region of the human X chromosome

1 reference

12 December 2020

Physical mapping of the cystic fibrosis region by pulsed-field gel electrophoresis

1 reference

12 December 2020

Clones from an 840-kb fragment containing the 5' region of the DMD locus enriched by pulsed field gel electrophoresis

1 reference

12 December 2020

Identifiers

PMCID

1682742

1 reference

7 August 2017

1 reference