(Q44986039)

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

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scholarly article

1 reference

Europe PubMed Central

8 December 2017

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

1 reference

Europe PubMed Central

8 December 2017

David F. Callen

1

1 reference

Europe PubMed Central

8 December 2017

Grant R Sutherland

4

object named as

G R Sutherland

1 reference

Europe PubMed Central

8 December 2017

author name string

J C Mulley

2

1 reference

Europe PubMed Central

8 December 2017

E G Baker

3

1 reference

Europe PubMed Central

8 December 2017

publication date

1 November 1987

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Europe PubMed Central

8 December 2017

1 reference

Europe PubMed Central

8 December 2017

77

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Europe PubMed Central

8 December 2017

236-240

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Europe PubMed Central

8 December 2017

3

1 reference

Europe PubMed Central

8 December 2017

https://scigraph.springernature.com/pub.10.1007/bf00284476

0 references

Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479386

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A male with a monocentric Yq isochromosome and presence of a Yp-specific DNA sequence

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479386

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/3479386

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage and genetic counselling for the fragile X using DNA probes 52A, F9, DX13, and ST14

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479386

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of the human haptoglobin genes distal to the fragile site at 16q22 using in situ hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479386

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

How do human isochromosomes arise?

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479386

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/3479386

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High-resolution chromosomal localization of human genes for amylase, proopiomelanocortin, somatostatin, and a DNA fragment (D3S1) by in situ hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479386

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Morphology alone does not make an isochromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3479386

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00284476

1 reference

Europe PubMed Central

8 December 2017

1 reference

Europe PubMed Central

8 December 2017

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