The marker (X) syndrome: a cytogenetic and genetic analysis. (Q52093239)

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scientific article published in January 1984

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Language	Label	Description	Also known as
English	The marker (X) syndrome: a cytogenetic and genetic analysis.	scientific article published in January 1984

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6712153

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6712153

title

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

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6712153

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6712153

author

Newton Ennis Morton

series ordinal

2

object named as

Morton NE

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6712153

retrieved

22 April 2018

author name string

Sherman SL

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6712153

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6712153

Jacobs PA

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6712153

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6712153

Turner G

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6712153

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6712153

language of work or name

English

0 references

publication date

1 January 1984

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6712153

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6712153

published in

Annals of Human Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6712153

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6712153

volume

48

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6712153

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6712153

issue

Pt 1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6712153

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6712153

page(s)

21-37

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6712153

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6712153

cites work

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

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1984.TB00830.X

retrieved

21 January 2018

Constitutional chromosomal breakage.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1984.TB00830.X

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1984.TB00830.X

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1984.TB00830.X

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1984.TB00830.X

retrieved

21 January 2018

Effect of inbreeding on IQ and mental retardation

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1984.TB00830.X

retrieved

21 January 2018

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

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1984.TB00830.X

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1984.TB00830.X

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1984.TB00830.X

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1984.TB00830.X

retrieved

21 January 2018

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

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1984.TB00830.X

retrieved

21 January 2018

Marker X chromosome induction in fibroblasts by FUdR

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1984.TB00830.X

retrieved

21 January 2018

Identifiers

DOI

10.1111/J.1469-1809.1984.TB00830.X

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6712153

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6712153

PubMed publication ID

6712153

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6712153

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6712153

 

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