(Q52107660)

English

Heritable fragile sites on human chromosomes. III. Detection of fra(X)(q27) in males with X-linked mental retardation and in their female relatives

scientific article published on January 1, 1979

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/535898

Heritable fragile sites on human chromosomes. III. Detection of fra(X)(q27) in males with X-linked mental retardation and in their female relatives (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A535898

10 July 2022

genetic carrier screening

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A535898

10 July 2022

author name string

G. R. Sutherland

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A535898

10 July 2022

language of work or name

1 reference

National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=535898

10 July 2022

publication date

1 January 1979

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/535898

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/535898

53

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/535898

1

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/535898

23-27

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/535898

Marker X chromosomes and mental retardation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/535898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial X-linked mental retardation with an X chromosome abnormality

1 reference

https://pubmed.ncbi.nlm.nih.gov/535898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium

1 reference

https://pubmed.ncbi.nlm.nih.gov/535898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carrier detection in X-linked mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/535898

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/535898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Constitutional chromosomal breakage.

1 reference

https://pubmed.ncbi.nlm.nih.gov/535898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial X-linked mental retardation, verbal disability, and marker X chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/535898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-Linked mental retardation with macro-orchidism and the fragile site at Xq27 or 28

1 reference

https://pubmed.ncbi.nlm.nih.gov/535898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial X-linked mental retardation with an X chromosome abnormality and macro-orchidism.

1 reference

https://pubmed.ncbi.nlm.nih.gov/535898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carrier detection in x-linked mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/535898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A marker X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/535898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Marker X chromosomes, mental retardation and macro-orchidism

1 reference

https://pubmed.ncbi.nlm.nih.gov/535898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carrier detection in X-linked mental retardation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/535898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heritable fragile sites on human chromosomes II. Distribution, phenotypic effects, and cytogenetics

1 reference

https://pubmed.ncbi.nlm.nih.gov/535898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00289445

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/535898

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

http://europepmc.org/abstract/MED/535898

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