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Assignment of anonymous DNA probes to specific intervals of human chromosomes 16 and X. (Q35564622)

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scientific article published on August 1989

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English	Assignment of anonymous DNA probes to specific intervals of human chromosomes 16 and X.	scientific article published on August 1989

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Assignment of anonymous DNA probes to specific intervals of human chromosomes 16 and X. (English)

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Ruth N MacKinnon

1 reference

ORCID Public Data File 2021

author name string

Hyland VJ

1

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Fernandez KE

2

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Callen DF

3

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

MacKinnon RN

4

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Baker E

5

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Friend K

6

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Sutherland GR

7

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

publication date

1 August 1989

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

language of work or name

0 references

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

83

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

61-66

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Report of the committee on cytogenetic markers

1 reference

https://pubmed.ncbi.nlm.nih.gov/2570019

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional assignment of genes for human α-globin and phosphoglycollate phosphatase to the short arm of chromosome 16

1 reference

https://pubmed.ncbi.nlm.nih.gov/2570019

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mouse-human hybrid cell panel for mapping human chromosome 16.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2570019

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human alpha-globin maps to pter-p13.3 in chromosome 16 distal to PGP

1 reference

https://pubmed.ncbi.nlm.nih.gov/2570019

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Anonymous DNA probes to human chromosome 16 derived from a flow-purified library.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2570019

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fine mapping of gene probes and anonymous DNA fragments to the long arm of chromosome 16

1 reference

https://pubmed.ncbi.nlm.nih.gov/2570019

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and localization of DNA segments from specific human chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2570019

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional localization of 18 human X-linked DNA sequences

1 reference

https://pubmed.ncbi.nlm.nih.gov/2570019

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of the fragile (X) chromosome in an interspecific somatic cell hybrid

1 reference

https://pubmed.ncbi.nlm.nih.gov/2570019

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping the short arm of human chromosome 16.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2570019

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2570019

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Removal of repeated sequences from hybridisation probes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2570019

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Efficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid-cell line: mapping of new probes close to the locus for X-linked mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/2570019

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage between the fragile X and F9, DXS52 (St14), DXS98 (4D-8) and DXS105 (cX55.7).

1 reference

https://pubmed.ncbi.nlm.nih.gov/2570019

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16

1 reference

https://pubmed.ncbi.nlm.nih.gov/2570019

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00274150

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

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