Genetic linkage heterogeneity in the fragile X syndrome (Q70096795)

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scientific article published on 01 January 1985

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Language	Label	Description	Also known as
English	Genetic linkage heterogeneity in the fragile X syndrome	scientific article published on 01 January 1985

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2993154

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2993154%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 October 2019

title

Genetic linkage heterogeneity in the fragile X syndrome (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2993154

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2993154%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 October 2019

main subject

heterogeneity

1 reference

based on heuristic

inferred from title

fragile X syndrome

1 reference

based on heuristic

inferred from title

author name string

W T Brown

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2993154

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2993154%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 October 2019

A C Gross

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2993154

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2993154%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 October 2019

C B Chan

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2993154

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2993154%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 October 2019

E C Jenkins

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2993154

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2993154%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 October 2019

publication date

1 January 1985

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2993154

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2993154%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 October 2019

published in

Human Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2993154

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2993154%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 October 2019

volume

71

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2993154

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2993154%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 October 2019

issue

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2993154

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2993154%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 October 2019

page(s)

11-18

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2993154

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2993154%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 October 2019

cites work

X-linked mental retardation with fragile X. A pedigree showing transmission by apparently unaffected males and partial expression in female carriers.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Constitutive fragile sites 1p31, 3p14, 6q26, and 16q23 and their use as controls for false-negative results with the fragile(X).

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile X syndrome: associated neurological abnormalities and developmental disabilities

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited congenital normofunctional testicular hyperplasia and mental deficiency

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linkage and genetic heterogeneity in bipolar-related major affective illness: reanalysis of linkage data

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The marker (X) syndrome: a cytogenetic and genetic analysis.

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism is associated with the fragile-X syndrome

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inversion in the H–2 complex of t-haplotypes in mice

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cytogenetic study of a population of mentally retarded males with special reference to the marker (X) syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening for fragile X syndrome by testicular size measurement

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage analysis of X-linked mental retardation with and without fragile-X using factor IX gene probe

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The strength of association between fragile (X) chromosome presence and mental retardation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Marker X-associated mental retardation. A study of 150 retarded males.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

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Conference report: International Workshop on the fragile X and X-linked mental retardation.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal breakage in normal and fragile X subjects using low folate culture conditions

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and characterization of a cDNA coding for human factor IX

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Low frequencies of apparently fragile X chromosomes in normal control cultures: a possible explanation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TESTING FOR HETEROGENEITY OF RECOMBINATION FRACTION VALUES IN HUMAN GENETICS

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation and selection in the marker (X) syndrome. A hypothesis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile X

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage and recombination between fragile X-linked mental retardation and the factor IX gene.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The search for heterogeneity in insulin-dependent diabetes mellitus (IDDM): linkage studies, two-locus models, and genetic heterogeneity

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A PEDIGREE OF MENTAL DEFECT SHOWING SEX-LINKAGE.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transmission of the marker X syndrome trait by unaffected males: conclusions from studies of large families.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Marker X syndrome in an oriental family with probable transmission by a normal male.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The fragile X chromosome in a large Indian kindred.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transmission of fragile (X)(q27) from normal male(s)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile X trait in a large kindred: transmission also through normal males

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Experience with prenatal fragile X detection

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2993154

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/BF00295659

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2993154

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2993154%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 October 2019

PubMed publication ID

2993154

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2993154

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2993154%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 October 2019

 

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