Fragile site Xq27 and mental retardation. Clinical and cytogenetic manifestation in heterozygotes and hemizygotes of five kindreds. (Q52100034)

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scientific article published in January 1982

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English	Fragile site Xq27 and mental retardation. Clinical and cytogenetic manifestation in heterozygotes and hemizygotes of five kindreds.	scientific article published in January 1982

Statements

instance of

scholarly article

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stated in

Europe PubMed Central

PubMed publication ID

6955257

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6955257

title

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

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6955257

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6955257

author name string

A Schmidt

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6955257

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6955257

publication date

1 January 1982

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6955257

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6955257

published in

Human Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6955257

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6955257

volume

60

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6955257

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6955257

issue

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6955257

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6955257

page(s)

322-327

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6955257

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6955257

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/6955257

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked mental retardation, macro-orchidism, and the Xq27 fragile site

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6955257

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial X-linked mental retardation with an X chromosome abnormality

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6955257

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Further delineation of X-linked mental retardation.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6955257

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression in lymphocyte and fibroblast culture of the fragile X chromosome: A new technical approach

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6955257

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6955257

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Significance of phenotypic and chromosomal abnormalities in X-linked mental retardation (Martin-Bell or Renpenning syndrome).

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6955257

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile X in a normal male: a cautionary tale

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6955257

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial X-linked mental retardation and fragile X chromosomes in two Swedish families.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6955257

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile sites in human chromosomes II: demonstration of the fragile site Xq27 in carriers of X-linked mental retardation.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6955257

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nonspecific X-linked mental retardation I: a review with information from 24 new families

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6955257

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 'fragile' X chromosome in the Martin-Bell-Renpenning syndrome and in males with other forms of familial mental retardation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6955257

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6955257

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6955257

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6955257

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked mental retardation: Transmission of the trait by an apparently unaffected male

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6955257

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sex linked mental deficiency, unusual facies, macroorchidism and fragile site on chromosome X (author's transl)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6955257

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6955257

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6955257

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6955257

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[X-linked mental retardation and X-chromosome fragile sites (author's transl)]

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6955257

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/BF00569212

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6955257

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6955257

PubMed publication ID

6955257

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6955257

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6955257

 

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