(Q33592932)

28 July 2017

Further evidence localising the gene for Hunter's syndrome to the distal region of the X chromosome long arm (English)

1 reference

28 July 2017

Roberts SH

1

1 reference

28 July 2017

Upadhyaya M

series ordinal

2

1 reference

28 July 2017

Sarfarazi M

series ordinal

3

1 reference

28 July 2017

Harper PS

series ordinal

4

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 May 1989

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

26

1 reference

28 July 2017

5

1 reference

28 July 2017

309-313

1 reference

Strategies for multilocus linkage analysis in humans

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015597

Hunter's disease in a girl: association with X:5 chromosomal translocation disrupting the Hunter gene

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015597

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015597

New Giemsa method for the differential staining of sister chromatids

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015597

The human genes for hemophilia A and hemophilia B flank the X chromosome fragile site at Xq27.3.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015597

Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015597

Two sisters with a distal deletion at the Xq26/Xq27 interface: DNA studies indicate that the gene locus for factor IX is present

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015597

Multilocus analysis of the fragile X 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=1015597

Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015597

Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X site.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015597

Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B families

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015597

The fragile X syndrome in a large family. III. Investigations on linkage of flanking DNA markers with the fragile site Xq27.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015597

A rapid banding technique for human chromosomes

21 June 2018

1 reference

12 December 2020

Report of the committee on the genetic constitution of the X and Y chromosomes

1 reference

12 December 2020

Analysis of the fragile-X chromosome: localization and detection of the fragile site in high resolution preparations

1 reference

12 December 2020

Localisation of the gene for Hunter syndrome on the long arm of X chromosome

1 reference

12 December 2020

Ten families with fragile X syndrome: linkage relationships with four DNA probes from distal Xq

1 reference

12 December 2020

Genetics of Hunter syndrome: carrier detection, new mutations, segregation and linkage analysis

1 reference

12 December 2020

Identifiers

PMCID

1015597

1 reference

28 July 2017

1 reference