(Q52079380)

English

Mental impairment in Martin-Bell syndrome is probably determined by interaction of several genes: simple explanation of phenotypic differences between unaffected and affected males with the same X chromosome.

scientific article published in March 1986

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scholarly article

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/3957348

Mental impairment in Martin-Bell syndrome is probably determined by interaction of several genes: simple explanation of phenotypic differences between unaffected and affected males with the same X chromosome. (English)

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/3957348

fragile X syndrome

1 reference

based on heuristic

inferred from title

author name string

P Steinbach

1

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/3957348

publication date

1 March 1986

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/3957348

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/3957348

72

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Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/3957348

248-252

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/3957348

3

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/3957348

https://scigraph.springernature.com/pub.10.1007/bf00291888

0 references

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3957348

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of the fragile site Xq27 in fibroblasts. II. Evidence for negative and positive clones from heterozygous females and possible relationship between frequency and phenotype.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3957348

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On the frequency of telomeric chromosomal changes induced by culture conditions suitable for fragile X expression

1 reference

https://pubmed.ncbi.nlm.nih.gov/3957348

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3957348

12 December 2020

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The diagnosis and frequency of X-linked conditions in a cohort of moderately retarded males with affected brothers

1 reference

https://pubmed.ncbi.nlm.nih.gov/3957348

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transmission of fragile (X) (q27) site from a male

1 reference

https://pubmed.ncbi.nlm.nih.gov/3957348

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterozygous expression of X-linked mental retardation and X-chromosome marker fra(X)(q27).

1 reference

https://pubmed.ncbi.nlm.nih.gov/3957348

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recurrent mutation pressure does not explain the prevalence of the marker (X) syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3957348

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Manifestation of the fragile site Xq27 in fibroblasts. IV. Clones from a heterozygous female do not manifest this site homogeneously on either the early or late replicating X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3957348

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile X in a normal male: a cautionary tale

1 reference

https://pubmed.ncbi.nlm.nih.gov/3957348

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/3957348

12 December 2020

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Unborn Children (Protection) Bill

1 reference

https://pubmed.ncbi.nlm.nih.gov/3957348

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of the fragile site Xq27 in fibroblasts. I. Detection of fra(X)(q27) in fibroblast clones from males with X-linked mental retardation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3957348

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3957348

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3957348

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

https://pubmed.ncbi.nlm.nih.gov/3957348

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

https://pubmed.ncbi.nlm.nih.gov/3957348

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3957348

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

https://pubmed.ncbi.nlm.nih.gov/3957348

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/3957348

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/3957348

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00291888

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/3957348

1 reference

Europe PubMed Central

21 April 2018

http://europepmc.org/abstract/MED/3957348

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