Case Report: A Rare Cytogenetic Variant of Monosomy 18p Syndrome as a Consequence of Whole-Arm Translocation between Chromosomes 13 and 18

Q: How can I download an article?

To download an article from SID, first log in to the site, search for the article title, and click on the 'Download Article' option.

Q: How can I download an ISI article?

To download an ISI article on SID, enter the keyword or article title in the search bar, view the relevant results, click on the desired article, and select the 'Download Article' option.

Q: How can I access the SID database?

To access the SID database, visit SID.ir, create an account, and log in to access scientific resources.

Q: Is downloading articles from SID free?

Some articles on SID are available for free, while others require payment. Details are specified on the article's page.

SAFAVI MOEINADIN; HAGHI ASHTIANI MOHAMMAD TAGHI; SHERVIN BADV REZA; AZARI YAM AILEEN; VASEI MOHAMMAD

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Journal Paper

Paper Information

Journal: ARCHIVES OF IRANIAN MEDICINE Year:2019 | Volume:22 | Issue:10 Page(s): 627-628

Download Full-Text

View:

131

Download:

Cites:

Information Journal Paper

Title

Case Report: A Rare Cytogenetic Variant of Monosomy 18p Syndrome as a Consequence of Whole-Arm Translocation between Chromosomes 13 and 18

Author(s)

Keywords

18p deletion syndrome

Genetic

Translocation

Abstract

Monosomy 18p syndrome is one of the prototypical examples of autosomal terminal deletions. This deletion can be the consequence of de novo deletions, malsegregation of a balanced parental Translocation, cryptic subtelomeric deletions or ring chromosome 18. The present case is a rare cytoGenetic variant of monosomy 18 as a consequence of whole-arm Translocation between chromosomes 13 and 18 which has been reported only three times previously.

Cites

No record.

References

No record.

Cite

APA: Copy

SAFAVI, MOEINADIN, HAGHI ASHTIANI, MOHAMMAD TAGHI, SHERVIN BADV, REZA, AZARI YAM, AILEEN, & VASEI, MOHAMMAD. (2019). Case Report: A Rare Cytogenetic Variant of Monosomy 18p Syndrome as a Consequence of Whole-Arm Translocation between Chromosomes 13 and 18. ARCHIVES OF IRANIAN MEDICINE, 22(10), 627-628. SID. https://sid.ir/paper/281880/en

Vancouver: Copy

SAFAVI MOEINADIN, HAGHI ASHTIANI MOHAMMAD TAGHI, SHERVIN BADV REZA, AZARI YAM AILEEN, VASEI MOHAMMAD. Case Report: A Rare Cytogenetic Variant of Monosomy 18p Syndrome as a Consequence of Whole-Arm Translocation between Chromosomes 13 and 18. ARCHIVES OF IRANIAN MEDICINE[Internet]. 2019;22(10):627-628. Available from: https://sid.ir/paper/281880/en

IEEE: Copy

MOEINADIN SAFAVI, MOHAMMAD TAGHI HAGHI ASHTIANI, REZA SHERVIN BADV, AILEEN AZARI YAM, and MOHAMMAD VASEI, “Case Report: A Rare Cytogenetic Variant of Monosomy 18p Syndrome as a Consequence of Whole-Arm Translocation between Chromosomes 13 and 18,” ARCHIVES OF IRANIAN MEDICINE, vol. 22, no. 10, pp. 627–628, 2019, [Online]. Available: https://sid.ir/paper/281880/en

Related Journal Papers

No record.

Related Seminar Papers

No record.

Related Plans

No record.

Recommended Workshops