(Q35830053)

English

Cytogenetic and clinical studies in gonadal dysgenesis with 46,X,Xt(qter leads to p221::p223 leads to qter) karyotype: review and phenotype/karyotype correlations

scientific article published in December 1980

In more languages

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scholarly article

1 reference

Europe PubMed Central

10 August 2017

Cytogenetic and clinical studies in gonadal dysgenesis with 46,X,Xt(qter leads to p221::p223 leads to qter) karyotype: review and phenotype/karyotype correlations (English)

1 reference

Europe PubMed Central

10 August 2017

0 references

gonadal dysgenesis

1 reference

based on heuristic

inferred from title

author name string

Ferraro M

1

1 reference

Europe PubMed Central

10 August 2017

De Capoa A

2

1 reference

Europe PubMed Central

10 August 2017

Mostacci C

3

1 reference

Europe PubMed Central

10 August 2017

Pelliccia F

4

1 reference

Europe PubMed Central

10 August 2017

Zulli P

5

1 reference

Europe PubMed Central

10 August 2017

Baldini MA

6

1 reference

Europe PubMed Central

10 August 2017

Di Nisio Q

7

1 reference

Europe PubMed Central

10 August 2017

language of work or name

0 references

publication date

1 December 1980

1 reference

Europe PubMed Central

10 August 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

10 August 2017

17

1 reference

Europe PubMed Central

10 August 2017

6

1 reference

Europe PubMed Central

10 August 2017

457-463

1 reference

Europe PubMed Central

10 August 2017

X/X translocation in a patient with Turner's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885922

11 July 2018

Familial x/x translocation: t(x;x)(p22;q13)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885922

11 July 2018

New Giemsa method for the differential staining of sister chromatids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885922

11 July 2018

Apparently isodicentric but functionally monocentric X chromosome in man.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885922

11 July 2018

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

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885922

11 July 2018

Center for Barr body condensation. A case of Turner's syndrome with 45,X/46,X,dic(X) (Xqter leads to p22::p22 leads to qter)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885922

11 July 2018

Fusion of two apparently intact human X chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885922

11 July 2018

Isodicentric X chromosome in a woman with characteristics of gonadal dysgenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885922

11 July 2018

Gonadotropin-Induced Pregnancy Following “Premature Ovarian Failure”

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885922

11 July 2018

Multiple cytogenetic methods used to identify a new structural rearrangement of the human X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885922

11 July 2018

Chronology of the replication of sex chromosome bands in lymphocytes of normal subjects and patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885922

11 July 2018

Four new cases of X-autosome translocation in man (author's transl)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885922

11 July 2018

A simple technique for demonstrating centromeric heterochromatin

1 reference

https://pubmed.ncbi.nlm.nih.gov/7205428

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Staining of human chromosomes with acridine orange after treatment with 5 bromodeoxyuridine]

1 reference

https://pubmed.ncbi.nlm.nih.gov/7205428

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fusion of the short arms of one X chromosome in a patient with gonadal dysgenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/7205428

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal X chromosomes in man: Origin, behavior and effects

1 reference

https://pubmed.ncbi.nlm.nih.gov/7205428

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A second example of telomeric fusion 2 X chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/7205428

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-X translocation in a patient with gonadal dysgenesis and the problem of phenotype-karyotype correlations

1 reference

https://pubmed.ncbi.nlm.nih.gov/7205428

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Both X chromosomes function before visible X-chromosome inactivation in female mouse embryos

1 reference

https://pubmed.ncbi.nlm.nih.gov/7205428

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A universal stain for the sex chromatin body

1 reference

https://pubmed.ncbi.nlm.nih.gov/7205428

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7205428

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.17.6.457

0 references

1 reference

Europe PubMed Central

10 August 2017

1 reference

Europe PubMed Central

10 August 2017

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