(Q45888985)

English

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.

scientific article published in September 1987

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scholarly article

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3502701

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. (English)

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3502701

Elena Maria Clotilde Raimondi

6

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3502701

author name string

I Oberlé

1

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3502701

G Camerino

2

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3502701

K Wrogemann

3

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3502701

B Arveiler

4

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3502701

A Hanauer

5

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3502701

J L Mandel

7

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3502701

publication date

1 September 1987

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3502701

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3502701

77

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3502701

60-65

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3502701

1

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3502701

https://scigraph.springernature.com/pub.10.1007/bf00284716

0 references

The prenatal detection of the fragile X chromosome: review of recent experience

1 reference

https://pubmed.ncbi.nlm.nih.gov/3502701

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques

1 reference

https://pubmed.ncbi.nlm.nih.gov/3502701

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage studies of X-linked mental retardation: high frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome).

1 reference

https://pubmed.ncbi.nlm.nih.gov/3502701

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetic linkage map of the human X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3502701

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/3502701

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3502701

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic mapping and diagnosis of haemophilia A achieved through a BclI polymorphism in the factor VIII gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/3502701

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus).

1 reference

https://pubmed.ncbi.nlm.nih.gov/3502701

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Further segregation analysis of the fragile X syndrome with special reference to transmitting males

1 reference

https://pubmed.ncbi.nlm.nih.gov/3502701

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency

1 reference

https://pubmed.ncbi.nlm.nih.gov/3502701

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report of the Committee on the Genetic Constitution of the X and Y Chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/3502701

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional localization of 18 human X-linked DNA sequences

1 reference

https://pubmed.ncbi.nlm.nih.gov/3502701

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Marker (X)-Linked Mental Retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/3502701

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytological mapping of the human glucose-6-phosphate dehydrogenase gene distal to the fragile-X site suggests a high rate of meiotic recombination across this site

1 reference

https://pubmed.ncbi.nlm.nih.gov/3502701

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3502701

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Easy calculations of lod scores and genetic risks on small computers

1 reference

https://pubmed.ncbi.nlm.nih.gov/3502701

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A TaqI RFLP in Xq26-Xqter detected by pX45h [HGM8 no. DXS100h]

1 reference

https://pubmed.ncbi.nlm.nih.gov/3502701

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Efficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid-cell line: mapping of new probes close to the locus for X-linked mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/3502701

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cytological map of the human X chromosome--evidence for non-random recombination

1 reference

https://pubmed.ncbi.nlm.nih.gov/3502701

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers

1 reference

https://pubmed.ncbi.nlm.nih.gov/3502701

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA linkage studies in the fragile X syndrome suggest genetic heterogeneity

1 reference

https://pubmed.ncbi.nlm.nih.gov/3502701

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An assessment of the use of flanking DNA markers for fra(X) syndrome carrier detection and prenatal diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/3502701

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two anonymous X-specific human sequences detecting restriction fragment length polymorphisms in region Xq26?qter

1 reference

https://pubmed.ncbi.nlm.nih.gov/3502701

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male

1 reference

https://pubmed.ncbi.nlm.nih.gov/3502701

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00284716

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3502701

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

17 December 2017

http://europepmc.org/abstract/MED/3502701

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