(Q33213012)

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Isolation of anonymous DNA markers for human chromosome 22q11 from a flow-sorted library, and mapping using hybrids from patients with DiGeorge syndrome.

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21 September 2019

Isolation of anonymous DNA markers for human chromosome 22q11 from a flow-sorted library, and mapping using hybrids from patients with DiGeorge syndrome (English)

1 reference

Europe PubMed Central

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21 September 2019

Andrew Marck Sharkey

1

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21 September 2019

Peter J Scambler

7

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21 September 2019

author name string

L McLaren

2

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21 September 2019

M Carroll

3

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21 September 2019

J Fantes

4

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21 September 2019

D Green

5

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21 September 2019

D Wilson

6

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21 September 2019

H J Evans

8

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21 September 2019

publication date

1 April 1992

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21 September 2019

1 reference

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21 September 2019

89

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21 September 2019

73-78

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21 September 2019

1

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21 September 2019

https://scigraph.springernature.com/pub.10.1007/bf00207046

0 references

Regionally restricted developmental defects resulting from targeted disruption of the mouse homeobox gene hox-1.5

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An anonymous single copy chromosome 22 clone, D22S10 (22c1-18) identifies an RFLP with PstI.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypoparathyroidism and T cell immune defect in a patient with 10p deletion syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role for the Wilms tumor gene in genital development?

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A deletion in chromosome 22 can cause DiGeorge syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Features of Turner's and DiGeorge's syndromes in a child with an X;22 translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiovascular anomalies in DiGeorge syndrome and importance of neural crest as a possible pathogenetic factor.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular studies of DiGeorge syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dispersed human immunoglobulin kappa light-chain genes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of 27 DNA markers to the region of human chromosome 22q11-pter deleted in patients with the DiGeorge syndrome and duplicated in the der22 syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional localization of the genes coding for human ACO2, ARSA, and NAGA on chromosome 22

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Features of di George syndrome in a child with 45,XX,-3,-22,+der(3),t(3;22)(p25;q11).

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel centromeric repetitive DNA from human chromosome 22.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Flow cytometry measurements of human chromosome kinetochore labeling

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The spectrum of the DiGeorge syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

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/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A subfamily of alphoid repetitive DNA shared by the NOR-bearing human chromosomes 14 and 22.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular cytogenetics: toward dissection of the contiguous gene syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interstitial deletion of chromosome 22 in a patient with the DiGeorge malformation sequence.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Forty four probands with an additional "marker" chromosome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic findings in a prospective series of patients with DiGeorge anomaly

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of the supernumerary chromosome in cat eye syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

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/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial DiGeorge syndrome and associated partial monosomy of chromosome 22

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The DiGeorge anomaly as a developmental field defect

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of anonymous, polymorphic DNA fragments from human chromosome 22q12-qter

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The neuroepithelioma breakpoint on chromosome 22 is proximal to the meningioma locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Construction of fifteen human chromosome-specific DNA libraries from flow-purified chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A somatic cell hybrid with a single human chromosome 22 corrects the defect in the CHO mutant (Ade-I) lacking adenylosuccinase activity.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1577468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00207046

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1577468%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1577468%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

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