Pericentric X inversion in dizygotic twins who differ in X chromosome inactivation and menstrual cycle function. (Q52100061)

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scientific article published in January 1982

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Language	Label	Description	Also known as
English	Pericentric X inversion in dizygotic twins who differ in X chromosome inactivation and menstrual cycle function.	scientific article published in January 1982

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6892018

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6892018

title

Pericentric X inversion in dizygotic twins who differ in X chromosome inactivation and menstrual cycle function. (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6892018

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6892018

main subject

menstrual cycle

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based on heuristic

inferred from title

author name string

E A Keitges

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6892018

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6892018

C G Palmer

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6892018

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6892018

D D Weaver

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6892018

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6892018

publication date

1 January 1982

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6892018

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6892018

published in

Human Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6892018

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6892018

volume

62

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6892018

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6892018

issue

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6892018

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6892018

page(s)

210-213

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stated in

Europe PubMed Central

PubMed publication ID

6892018

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6892018

cites work

Turner's syndrome with a duplication-deficiency X chromosome derived from a maternal pericentric inversion X chromosome

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6892018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural X-chromosome abnormality in a female with gonadal dysgenesis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6892018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparison of thymidine, fluorodeoxyuridine, hydroxyurea, and methotrexate blocking at the G1/S phase transition of the cell cycle, studied by replication patterns

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6892018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

THE LYON-BEUTLER HYPOTHESIS AND ISOCHROMOSOME X PATIENTS WITH TURNER SYNDROME

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6892018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Follow-up on a human X-autosome translocation first studied in 1963 and 1964

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6892018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Demonstration of replication patterns corresponding to G- and R-type banding of chromosomes after partial sunchronization of cell cultures with BrdU or dT surplus

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6892018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recombinant chromosome as a result of pericentric inversion of X chromosome

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6892018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High Resolution of Human Chromosomes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6892018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial incidence of pericentric inversion of X chromosome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6892018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dermatoglyphics in medicine--problems and use in suspected chromosome abnormalities

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6892018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Banding patterns and autoradiographic studies of cells with an X-autosome translocation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6892018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X inactivation in man: a woman with t(Xq--;12q+)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6892018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Letter: A case of primary amenorrhea associated with X-autosomal translocation (46,X,t(Xq minus;5q plus))

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6892018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotypically normal individuals with an inversion (X) (p22q13) and the recombinant (X), dup q

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6892018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-autosome translocations: a review

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6892018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BrdU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6892018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A possible exception to the critical region hypothesis.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6892018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gonadal dysgenesis, intra-X chromosome insertion, and possible position effect in an otherwise normal female.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6892018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X chromosome constitution and the human female phenotype

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6892018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/BF00333520

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6892018

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6892018

PubMed publication ID

6892018

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6892018

retrieved

22 April 2018

reference URL

http://europepmc.org/abstract/MED/6892018

 

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