Abnormal X chromosomes in man: Origin, behavior and effects (Q68930452)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4475024 AND SRC:MED&resulttype=core&format=json

28 September 2019

title

Abnormal X chromosomes in man: origin, behavior and effects (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4475024 AND SRC:MED&resulttype=core&format=json

https://api.crossref.org/works/10.1007/BF00281002

28 September 2019

Abnormal X chromosomes in man: Origin, behavior and effects (English)

1 reference

22 January 2023

main subject

chromosome abnormality

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:4475024

sex chromosome aberration

22 January 2023

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:4475024

chromosomal translocation

22 January 2023

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:4475024

22 January 2023

author name string

E. Therman

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:4475024

22 January 2023

K. Patau

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:4475024

22 January 2023

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=4475024

22 January 2023

publication date

1 January 1974

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full work available at URL

28 September 2019

https://link.springer.com/content/pdf/10.1007/BF00281002.pdf

1 reference

https://api.crossref.org/works/10.1007/BF00281002

https://link.springer.com/article/10.1007/BF00281002/fulltext.html

22 January 2023

1 reference

https://api.crossref.org/works/10.1007/BF00281002

22 January 2023

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4475024 AND SRC:MED&resulttype=core&format=json

28 September 2019

volume

25

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28 September 2019

issue

1

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28 September 2019

page(s)

1-16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4475024 AND SRC:MED&resulttype=core&format=json

Duplication of an X chromosome in a case of Turner's syndrome (45,X-46,XXp )

28 September 2019

cites work

1 reference

12 December 2020

[46, XXip karyotype in a woman with normal stature and gonadal dysgenesis without other congenital anomalies]

1 reference

12 December 2020

A CASE OF PRIMARY AMENORRHEA WITH A TRANSLOCATION INVOLVING CHROMOSOMES OF GROUPS B AND C

1 reference

12 December 2020

Cytological mapping of human X-linked genes by use of somatic cell hybrids involving an X-autosome translocation (mouse-hamster-human X-linked markers).

1 reference

12 December 2020

Multiple abnormalities due to possible genetic inactivation in an X-autosome translocation.

1 reference

12 December 2020

Two human X-autosome translocations identified by autoradiography and fluorescence

1 reference

12 December 2020

Increased Q fluorescence of an inactive Xq-chromosome in man

1 reference

12 December 2020

Somatic stigmata of Turner's syndrome in a patient with 46,XXq-

1 reference

12 December 2020

Trisomy 13 with a 13-X translocation

1 reference

12 December 2020

1 reference

12 December 2020

Microfluorometric detection of deoxyribonucleic acid replication in human metaphase chromosomes

1 reference

12 December 2020

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

1 reference

12 December 2020

Cytogenetic and clinical study on 100 cases of primary amenorrhoea

1 reference

12 December 2020

X-autosome translocation in normal mother and effectively 21-monosomic daughter.

1 reference

12 December 2020

Unbalanced X-autosomal translocation with inactivation of the normal X chromosome

1 reference

12 December 2020

Evidence for X/X chromosome translocation in humans

1 reference

12 December 2020

Xq- Turner's syndrome: reconsideration of hypothesis that Xp- causes somatic features in Turner's syndrome

1 reference

12 December 2020

Non-Random Late Replication of X Chromosomes in Mules and Hinnies

1 reference

12 December 2020

An inhertited X‐autosome translocation in man

1 reference

12 December 2020

Center for Barr body condensation on the proximal part of the human Xq: a hypothesis

1 reference

12 December 2020

Apparently isodicentric but functionally monocentric X chromosome in man.

1 reference

12 December 2020

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

1 reference

12 December 2020

[Turner syndrome 45,X-46,XXq ]

1 reference

12 December 2020

Gonadal Dysgenesis with Unusual Abnormalities

1 reference

12 December 2020

Fluorescence and Giemsa banding studies of the allocyclic X chromosome in embryonic and adult mouse cells.

1 reference

12 December 2020

Pericentric inversion in a group D chromosome (13?15) associated with amenorrhea and gonadal dysgenesis

1 reference

12 December 2020

X-autosome translocations in the mouse: total inactivation versus partial inactivation of the X chromosome

1 reference

12 December 2020

A marker X chromosome

1 reference

12 December 2020

Autoradiographic studies on X-autosomal translocation in man: 45,X.15-,tan(15qZq )

1 reference

12 December 2020

Presumptive X-Autosome Translocation in a Cow : Preferential Inactivation of the Normal X Chromosome

1 reference

12 December 2020

Inactivation of the x-chromosome

1 reference

12 December 2020

The single-active-X: functional differentiation at the chromosome level

1 reference

12 December 2020

The nature of structural X chromosome aberrations in Turner's syndrome as revealed by quinacrine mustard fluorescence analysis

1 reference

12 December 2020

Gonadal dysgenesis with an unusual structural anomaly in an X chromosome (45,X-46,XXq )

1 reference

12 December 2020

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

1 reference

12 December 2020

Cytogenetics of fifty patients with primary amenorrhea

1 reference

12 December 2020

Anomalies of development in a girl with unusual sex chromosomal mosaicism

1 reference

12 December 2020

Autoradiographic investigations of centric fragments and rings in patients with stigmata of gonadal dysgenesis

1 reference

12 December 2020

A VERY LARGE METACENTRIC CHROMOSOME IN A WOMAN WITH SYMPTOMS OF TURNER'S SYNDROME

1 reference

12 December 2020

Genetic activity of sex chromosomes in somatic cells of mammals

1 reference

12 December 2020

An abnormal large human chromosome identified as an end-to-end fusion of two X's by combined results of the new banding techniques and microdensitometry.

1 reference

12 December 2020

Possible X-autosomal translocation in a girl with gonadal dysgenesis

1 reference

12 December 2020

Isochromosome for the short arm of X, a human 46, XXpi syndrome

1 reference

12 December 2020

[X-CHROMOSOME ANOMALY AND AHAPTOGLOBINEMIA IN HEMOPHILIA A]

1 reference

12 December 2020

X-chromosome inactivation and the Xg locus

1 reference

12 December 2020

Ring chromosomes and centric fragments in Turner's syndrome

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00281002

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=4475024

22 January 2023

1 reference