(Q33679473)

28 July 2017

1 reference

title

Interstitial duplication of the short arm of chromosome 2: report of a new case and review (English)

1 reference

28 July 2017

Mégarbané A

1

1 reference

28 July 2017

Souraty N

2

1 reference

28 July 2017

Prieur M

3

1 reference

28 July 2017

Theophile D

4

1 reference

28 July 2017

Chédid P

5

1 reference

28 July 2017

Augé J

6

1 reference

28 July 2017

Vekemans M

7

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 September 1997

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

34

1 reference

28 July 2017

783-786

1 reference

28 July 2017

9

1 reference

Agenesis of the lung associated with a chromosome abnormality (46,XX,2p+)

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051069

A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051069

Partial duplication of the short arm of chromosome 2 (dup(2)(p13----p21) associated with mental retardation and an Aarskog-like phenotype

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051069

Direct duplication 2p14?2p23

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051069

Clinical syndromes associated with partial duplications of chromosomes 2 and 3: dup(2p),dup(2q),dup(3p),dup(3q)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051069

Partial trisomy 2p due to a familial translocation 2/6. Cytogenetic and clinical case with special reference to ophthalmologic changes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051069

Duplication and deletion of chromosome band 2(p21p22) resulting from a familial interstitial insertion (2;11)(p21;p15).

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051069

Familial reciprocal translocation, t(2;10)(p24;q26), resulting in duplication 2p and delection 10q.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051069

Variable phenotype associated with duplication of different regions of 2p.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051069

[Familial 2-C translocation: 46,XYt(2p-;Cp+) and 46,XXCp+].

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051069

Equilibrated 2-14 translocation in a mother and partial trisomy of a pair of the short branches of a number 2 chromosome in 2 of her children

30 October 2018

1 reference

12 December 2020

The 2p partial trisomy syndrome. Duplication of region 2p23 leads to 2pter in two members of a t(2;7) translocation kindred

1 reference

12 December 2020

Anterior segment mesenchymal dysgenesis associated with partial duplication of the short arm of chromosome 2

1 reference

12 December 2020

Multiple congenital anomalies due to partial 2p13----2pter duplication resulting from an unbalanced X;2 translocation

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.34.9.783

1 reference

28 July 2017

1 reference

28 July 2017

1 reference