(Q41725459)

English

Pericentromeric structure of human X "isochromosomes": evidence for molecular heterogeneity

scientific article published on August 1990

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

Pericentromeric structure of human X "isochromosomes": evidence for molecular heterogeneity (English)

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

author name string

C B Sharp

1

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

H M Bedford

2

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

H F Willard

3

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

publication date

1 August 1990

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

85

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Europe PubMed Central

PubMed publication ID

8 October 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

330-336

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

The human neurofilament gene (NEFL) is located on the short arm of chromosome 8.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2394446

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isochromosome-X in man. I

1 reference

https://pubmed.ncbi.nlm.nih.gov/2394446

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dicentric human X chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2394446

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular studies of the parental origin and nature of human X isochromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2394446

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic findings in 89 cases of Turner's syndrome with abnormal karyotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2394446

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

https://pubmed.ncbi.nlm.nih.gov/2394446

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

https://pubmed.ncbi.nlm.nih.gov/2394446

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alphoid satellite DNA is tightly associated with centromere antigens in human chromosomes throughout the cell cycle

1 reference

https://pubmed.ncbi.nlm.nih.gov/2394446

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/2394446

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cloned sequence, p82H, of the alphoid repeated DNA family found at the centromeres of all human chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2394446

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome-specific organization of human alpha satellite DNA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2394446

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal localization of complex and simple repeated human DNAs

1 reference

https://pubmed.ncbi.nlm.nih.gov/2394446

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and characterization of a major tandem repeat family from the human X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2394446

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Determining the origin of human X isochromosomes by use of DNA sequence polymorphisms and detection of an apparent i(Xq) with Xp sequences

1 reference

https://pubmed.ncbi.nlm.nih.gov/2394446

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic analysis of the proximal region of chromosome 2 of Drosophila melanogaster. I. Detachment products of compound autosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2394446

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dicentric chromosomes and the inactivation of the centromere

1 reference

https://pubmed.ncbi.nlm.nih.gov/2394446

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The distribution of chromosomal genotypes associated with Turner's syndrome: livebirth prevalence rates and evidence for diminished fetal mortality and severity in genotypes associated with structural X abnormalities or mosaicism

1 reference

https://pubmed.ncbi.nlm.nih.gov/2394446

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal and clinical findings in 110 females with Turner syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2394446

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An X,isochromosome X (long arm), 46 chromosomes. Human Genetic Mutant Cell Repository, Camden, N.J., identification No. GM-88

1 reference

https://pubmed.ncbi.nlm.nih.gov/2394446

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00206757

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

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0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

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