(Q34048454)

English

Down syndrome with duplication of a region of chromosome 21 containing the CuZn superoxide dismutase gene without detectable karyotypic abnormality

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scholarly article

1 reference

Europe PubMed Central

30 July 2017

Down syndrome with duplication of a region of chromosome 21 containing the CuZn superoxide dismutase gene without detectable karyotypic abnormality (English)

1 reference

Europe PubMed Central

30 July 2017

1 reference

based on heuristic

inferred from title

author name string

Huret JL

1

1 reference

Europe PubMed Central

30 July 2017

Delabar JM

2

1 reference

Europe PubMed Central

30 July 2017

Marlhens F

3

1 reference

Europe PubMed Central

30 July 2017

Aurias A

4

1 reference

Europe PubMed Central

30 July 2017

Nicole A

5

1 reference

Europe PubMed Central

30 July 2017

Berthier M

6

1 reference

Europe PubMed Central

30 July 2017

Tanzer J

7

1 reference

Europe PubMed Central

30 July 2017

Sinet PM

8

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Europe PubMed Central

30 July 2017

publication date

1 March 1987

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Europe PubMed Central

30 July 2017

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Europe PubMed Central

30 July 2017

75

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30 July 2017

251-257

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30 July 2017

3

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30 July 2017

https://scigraph.springernature.com/pub.10.1007/bf00281069

0 references

SOD-A and chromosome 21. Conflicting findings in a familial translocation (9p24;21q214)

1 reference

https://pubmed.ncbi.nlm.nih.gov/2951317

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trisomy 21 for the region 21q223: identification by high-resolution R-banding patterns

1 reference

https://pubmed.ncbi.nlm.nih.gov/2951317

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial trisomies of chromosome 21 in man. Two new observations due to translocations 19;21 and 4;21

1 reference

https://pubmed.ncbi.nlm.nih.gov/2951317

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for a correlation between late replication and autosomal gene inactivation in a familial translocation t(X;21)

1 reference

https://pubmed.ncbi.nlm.nih.gov/2951317

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human cytoplasmic superoxide dismutase cDNA clone: a probe for studying the molecular biology of Down syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2951317

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Atypical Down syndrome and partial trisomy 21

1 reference

https://pubmed.ncbi.nlm.nih.gov/2951317

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial Down syndrome due to t(10;21) translocation: evidence that the Down phenotype is related to trisomy of a specific segment of chromosome 21

1 reference

https://pubmed.ncbi.nlm.nih.gov/2951317

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Confirmation of the assignment of the human SODS gene to chromosome 21q22.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2951317

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Down's syndrome phenotype and autosomal gene inactivation in a child with presumed (X;21) de novo translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/2951317

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial trisomy 21

1 reference

https://pubmed.ncbi.nlm.nih.gov/2951317

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Partial trisomy for the segment 21(q11----qter) resulting from a de novo translocation between chromosomes 5 and 21]

1 reference

https://pubmed.ncbi.nlm.nih.gov/2951317

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/2951317

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nucleotide sequence and expression of human chromosome 21-encoded superoxide dismutase mRNA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2951317

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial trisomy 21 (21q21 - 21q22.2)

1 reference

https://pubmed.ncbi.nlm.nih.gov/2951317

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Superoxide dismutase: improved assays and an assay applicable to acrylamide gels

1 reference

https://pubmed.ncbi.nlm.nih.gov/2951317

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Down's syndrome. The possibility of a pathogenetic segment on chromosome no. 21.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2951317

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trisomy 21 and superoxide dismutase-1 (IPO-A). Tentative localization of sub-band 21Q22.1

1 reference

https://pubmed.ncbi.nlm.nih.gov/2951317

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA probe localization at 18p113 band by in situ hybridization and identification of a small supernumerary chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2951317

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/2951317

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Moderate Down's syndrome in three siblings having partial trisomy 21q22.2?qter and therefore no SOD-1 excess

1 reference

https://pubmed.ncbi.nlm.nih.gov/2951317

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New Giemsa method for the differential staining of sister chromatids

1 reference

https://pubmed.ncbi.nlm.nih.gov/2951317

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00281069

1 reference

Europe PubMed Central

30 July 2017

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0 references

1 reference

Europe PubMed Central

30 July 2017

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