The turner phenotype and the different types of human X isochromsome (Q70762067)

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scientific article published on 01 January 1981

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English	The turner phenotype and the different types of human X isochromsome	scientific article published on 01 January 1981

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7228026

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7228026%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 October 2019

title

The Turner phenotype and the different types of human x isochromosome (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7228026

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7228026%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 October 2019

The turner phenotype and the different types of human X isochromsome (English)

1 reference

stated in

Crossref

DOI

10.1007/BF00282013

reference URL

https://api.crossref.org/works/10.1007/BF00282013

retrieved

13 March 2024

main subject

phenotype

1 reference

based on heuristic

inferred from title

genetics

1 reference

stated in

Crossref

DOI

10.1007/BF00282013

reference URL

https://api.crossref.org/works/10.1007/BF00282013

retrieved

13 March 2024

author name string

P. G. Otto

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7228026

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7228026

retrieved

13 March 2024

A. M. Vianna-Morgante

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7228026

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7228026

retrieved

13 March 2024

P. A. Otto

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7228026

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7228026

retrieved

13 March 2024

A. Wajntal

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7228026

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7228026

retrieved

13 March 2024

language of work or name

English

1 reference

stated in

National Center for Biotechnology Information

PubMed publication ID

7228026

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7228026

retrieved

13 March 2024

publication date

1 January 1981

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7228026

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7228026%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 October 2019

full work available at URL

http://link.springer.com/content/pdf/10.1007/BF00282013.pdf

file format

Portable Document Format

1 reference

stated in

Crossref

DOI

10.1007/BF00282013

reference URL

https://api.crossref.org/works/10.1007/BF00282013

retrieved

13 March 2024

http://link.springer.com/article/10.1007/BF00282013/fulltext.html

file format

HTML

1 reference

stated in

Crossref

DOI

10.1007/BF00282013

reference URL

https://api.crossref.org/works/10.1007/BF00282013

retrieved

13 March 2024

http://link.springer.com/content/pdf/10.1007/BF00282013

1 reference

stated in

Crossref

DOI

10.1007/BF00282013

reference URL

https://api.crossref.org/works/10.1007/BF00282013

retrieved

13 March 2024

published in

Human Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7228026

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7228026%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 October 2019

volume

57

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7228026

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7228026%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 October 2019

issue

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7228026

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7228026%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 October 2019

page(s)

159-164

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7228026

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7228026%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 October 2019

cites work

46, X,X-X terminal rearrangement/45, X mosaicism in a child with short stature

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dicentric X isochromosomes in man

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Replication patterns of three isodicentric X chromosomes and an X isochromosome in human lymphocytes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dicentric human X chromosomes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic studies in seven individuals with an i(Xq) karyotype

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A second example of telomeric fusion 2 X chromosomes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural aberrations of the X chromosome in man

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Number of C-bands of human isochromosome Xqi and relation to 45,X mosaicism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytological findings of 10 cases with i(Xq) and one with dic(X)(qter leads to cen leads to p22::p11 leads to qter)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dicentric X-isochromosome (Xqi dic) and pericentric inversion of No. 2 inv(2) (p15) q21) in a patient with gonadal dysgenesis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a large submetacentric X chromosome as pericentric inversion of an isochromosome of the long arm

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differences in human X isochromosomes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isochromosome X in man: different DNA replication patterns in the long arms

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Replication and inactivation of a dicentric X formed by telomeric fusion

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal sex in ovarian agenesis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cell division and sister chromatid exchanges in 45,X/46,Xi(Xq) mosaicism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Symptoms of Turner's syndrome and interstitial heterochromatin in i(Xq)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ovarian dysgenesis due to 45 X, 0/46 dic (X) mosaicism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple technique for demonstrating centromeric heterochromatin

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Duplication Deficiency of an X-Chromosome with and Without 45,X Mosaicism in Three Girls — Cytogenetic, Clinical, and Hormonal Findings

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A girl with mosaicism for a dicentric X chromosome (45,X/46,X,dic(X) (Xqter to p22::p22 to qter))

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal and clinical findings in 110 females with Turner syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Further dicentric X isochromosomes and deletions, and a new structure i(X)(pter to q2102 to pter)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A rapid banding technique for human chromosomes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

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/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A girl with an end-to-end fusion of two X's

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An abnormal dicentric X chromosome in a patient with short stature and gonadal dysgenesis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal sex in Turner's syndrome with coarctation of the aorta

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7228026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/BF00282013

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7228026

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7228026%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 October 2019

PubMed publication ID

7228026

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7228026

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7228026%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 October 2019

 

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