Isodicentric X chromosome in a moderately tall patient with gonadal dysgenesis: lack of effect of functional centromere on inactivation pattern. (Q33670048)

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English	Isodicentric X chromosome in a moderately tall patient with gonadal dysgenesis: lack of effect of functional centromere on inactivation pattern.	scientific article

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scholarly article

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7154045%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

Isodicentric X chromosome in a moderately tall patient with gonadal dysgenesis: lack of effect of functional centromere on inactivation pattern (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7154045%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

gonadal dysgenesis

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J Robertson

1

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12 October 2019

M J Faed

2

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12 October 2019

M A Lamont

3

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12 October 2019

A M Crowder

4

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12 October 2019

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1 December 1982

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12 October 2019

Journal of Medical Genetics

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12 October 2019

19

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12 October 2019

6

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12 October 2019

463-465

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12 October 2019

Replication and inactivation of a dicentric X formed by telomeric fusion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048964

21 June 2018

Female phenotype and multiple abnormalities in sibs with a Y chromosome and partial X chromosome duplication: H--Y antigen and Xg blood group findings

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048964

21 June 2018

X chromosomes attached by their short arm : presence of an inactive centromere influences the replication patterns

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048964

21 June 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=1048964

21 June 2018

A case of long arm deletion of the X chromosome in a patient with secondary amenorrhea

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048964

21 June 2018

Partial long arm deletion of one X chromosome in a patient with secondary amenorrhea

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048964

21 June 2018

X chromosomes attached by their long arm: replication autonomy of the short arm adjacent to the inactive centromere

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048964

21 June 2018

Letter: Cytogenetic evidence for evolution of X-chromosome inactivation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048964

21 June 2018

A rapid banding technique for human chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/7154045

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple technique for demonstrating centromeric heterochromatin

1 reference

https://pubmed.ncbi.nlm.nih.gov/7154045

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Presumptive evidence of two active X chromosomes in somatic cells of a human female

1 reference

https://pubmed.ncbi.nlm.nih.gov/7154045

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Women heterozygous for deficiency of the (p21 ? pter) region of the X chromosome are fertile

1 reference

https://pubmed.ncbi.nlm.nih.gov/7154045

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

https://pubmed.ncbi.nlm.nih.gov/7154045

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited interstitial del(Xp) with minimal clinical consequences: with a note on the location of genes controlling phenotypic features

1 reference

https://pubmed.ncbi.nlm.nih.gov/7154045

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tandem duplication dup(X)(q13q22) in a male proband inherited from the mother showing mosaicism of X-inactivation

1 reference

https://pubmed.ncbi.nlm.nih.gov/7154045

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/7154045

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.19.6.463

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7154045%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7154045%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7154045%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

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