(Q35570049)

8 August 2017

title

Apparently isodicentric but functionally monocentric X chromosome in man. (English)

1 reference

8 August 2017

Therman E

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8 August 2017

Sarto GE

series ordinal

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8 August 2017

Patau K

series ordinal

1 reference

8 August 2017

language of work or name

English

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publication date

1 January 1974

1 reference

American Journal of Human Genetics

8 August 2017

published in

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8 August 2017

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8 August 2017

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8 August 2017

page(s)

83-92

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Anomalies of development in a girl with unusual sex chromosomal mosaicism

8 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762552

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762552

Two human X-autosome translocations identified by autoradiography and fluorescence

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762552

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762552

A stable human dicentric chromosome, t dic (12;14)(p13;p13) including an intercalary satellite region between centromeres

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762552

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762552

Polymorphism of human C-band heterochromatin. I. Frequency of variants

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762552

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.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762552

Quantitative karyotyping: a model twin study

12 July 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Multiple congenital anomalies associated with a ring 3 chromosome and translocated 3/X chromosome

1 reference

12 December 2020

A 45, XX,5–,13–, dic+ karyotype in a case of cri-du-chat syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Dicentric and monocentric Robertsonian translocations in man

1 reference

12 December 2020

Identifiers

PMC publication ID

1762552

1 reference

8 August 2017

1 reference