(Q33597886)

English

Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site

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scholarly article

1 reference

Europe PubMed Central

28 July 2017

Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site (English)

1 reference

Europe PubMed Central

28 July 2017

1 reference

based on heuristic

inferred from title

fragile X syndrome

1 reference

based on heuristic

inferred from title

4

object named as

E Kremer

1 reference

Europe PubMed Central

28 July 2017

Grant R Sutherland

9

object named as

G R Sutherland

1 reference

Europe PubMed Central

28 July 2017

author name string

R I Richards

1

1 reference

Europe PubMed Central

28 July 2017

K Holman

2

1 reference

Europe PubMed Central

28 July 2017

H Kozman

3

1 reference

Europe PubMed Central

28 July 2017

M Lynch

5

1 reference

Europe PubMed Central

28 July 2017

M Pritchard

6

1 reference

Europe PubMed Central

28 July 2017

S Yu

7

1 reference

Europe PubMed Central

28 July 2017

J Mulley

8

1 reference

Europe PubMed Central

28 July 2017

language of work or name

0 references

publication date

1 December 1991

1 reference

Europe PubMed Central

28 July 2017

Journal of Medical Genetics

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Europe PubMed Central

28 July 2017

28

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Europe PubMed Central

28 July 2017

818-823

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Europe PubMed Central

28 July 2017

12

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Europe PubMed Central

28 July 2017

Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017157

21 June 2018

Fragile X syndrome: diagnosis using highly polymorphic microsatellite markers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017157

21 June 2018

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017157

21 June 2018

Human glandular kallikrein genes: Genetic and physical mapping of the KLK1 locus using a highly polymorphic microsatellite PCR marker

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017157

21 June 2018

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017157

21 June 2018

Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017157

21 June 2018

Genetic mapping of new RFLPs at Xq27–q28

1 reference

https://pubmed.ncbi.nlm.nih.gov/1757956

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.28.12.818

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

28 July 2017

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