(Q52100061)

English

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

scientific article published in January 1982

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Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

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

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

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

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

menstrual cycle

1 reference

based on heuristic

inferred from title

author name string

E A Keitges

1

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

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

C G Palmer

2

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

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

D D Weaver

3

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

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

publication date

1 January 1982

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

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

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

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

62

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

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

3

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

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

210-213

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

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

https://scigraph.springernature.com/pub.10.1007/bf00333520

0 references

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

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural X-chromosome abnormality in a female with gonadal dysgenesis

1 reference

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

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

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

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

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

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

1 reference

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

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

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recombinant chromosome as a result of pericentric inversion of X chromosome

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High Resolution of Human Chromosomes

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial incidence of pericentric inversion of X chromosome

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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

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

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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

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

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

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

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-autosome translocations: a review

1 reference

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

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

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A possible exception to the critical region hypothesis.

1 reference

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

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

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X chromosome constitution and the human female phenotype

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00333520

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

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

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

22 April 2018

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

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