(Q52093410)

English

Heterozygous female carriers of the marker-X-chromosome: IQ estimation and replication status of fra(X)(q).

scientific article published in January 1984

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6586635

Heterozygous female carriers of the marker-X-chromosome: IQ estimation and replication status of fra(X)(q). (English)

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6586635

1 reference

based on heuristic

inferred from title

author name string

J Paul

1

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6586635

U Froster-Iskenius

2

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6586635

W Moje

3

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6586635

E Schwinger

4

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6586635

publication date

1 January 1984

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6586635

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6586635

66

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6586635

4

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6586635

344-346

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6586635

https://scigraph.springernature.com/pub.10.1007/bf00287638

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/6586635

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The fragile X(q27) form of X-linked mental retardation: FUdR as an inducing agent for fra(X)(q27) expression in lymphocytes, fibroblasts, and amniocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/6586635

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Additional evidence for fragile X activity in heterozygous carriers.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6586635

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening for fra(X)(q) in a population of mentally retarded males.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6586635

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carrier detection and X-inactivation studies in the fragile X syndrome. Cytogenetic studies in 63 obligate and potential carriers of the fragile X.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6586635

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/6586635

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile (X)(q27) sites in a pedigree with female carriers showing mild to severe mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/6586635

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile site Xq27 and mental retardation. Clinical and cytogenetic manifestation in heterozygotes and hemizygotes of five kindreds.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6586635

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Replication status of the fragile X chromosome, fra(X)(q27), in three heterozygous females.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6586635

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile X-linked mental retardation. A survey of 65 patients with mental retardation of unknown origin.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6586635

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heritable fragile sites on human chromosomes I. Factors affecting expression in lymphocyte culture

1 reference

https://pubmed.ncbi.nlm.nih.gov/6586635

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Short forms of a short psychopathological intelligence test (author's transl)

1 reference

https://pubmed.ncbi.nlm.nih.gov/6586635

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Activity of the fragile X in heterozygous carriers

1 reference

https://pubmed.ncbi.nlm.nih.gov/6586635

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked mental retardation: a study of 7 families.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6586635

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile (X) X-linked mental retardation I: relationship between age and intelligence and the frequency of expression of fragil (X)(q28).

1 reference

https://pubmed.ncbi.nlm.nih.gov/6586635

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked mental retardation with macro-orchidism and marker X chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/6586635

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked mental retardation with macro-orchidism and marker-X chromosomes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6586635

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Replication pattern in XXY cells with fra(X)

1 reference

https://pubmed.ncbi.nlm.nih.gov/6586635

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00287638

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6586635

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/6586635

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