(Q35198452)

7 August 2017

Allan-Herndon syndrome. II. Linkage to DNA markers in Xq21 (English)

1 reference

7 August 2017

Schwartz CE

1

1 reference

7 August 2017

Ulmer J

2

1 reference

7 August 2017

Brown A

3

1 reference

7 August 2017

Pancoast I

4

1 reference

7 August 2017

Goodman HO

5

1 reference

7 August 2017

Stevenson RE

6

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 September 1990

1 reference

American Journal of Human Genetics

7 August 2017

1 reference

7 August 2017

47

1 reference

7 August 2017

3

1 reference

7 August 2017

454-458

1 reference

Easy calculations of lod scores and genetic risks on small computers

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683855

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683855

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683855

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683855

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683855

A polymorphic human myosin heavy chain locus is linked to an anonymous single copy locus (D17S1) at 17p13

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683855

Report of the committee on linkage and gene order

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683855

MASA syndrome: further clinical delineation and chromosomal localisation

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683855

Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683855

A probe from an X-Y homology region detects RFLPs in Xq13-q22.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683855

Allan-Herndon syndrome. I. Clinical studies

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683855

Fragile X-linked mental retardation: the Martin-Bell syndrome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683855

A new X-linked syndrome with muscle atrophy, congenital contractures, and oculomotor apraxia

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683855

Genetic mapping of nine DNA markers in the q11----q22 region of the human X chromosome

26 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2393020

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMCID

1683855

1 reference

7 August 2017

1 reference