Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian P...
Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian Patients with Multiple Congenital Anomalies
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Author / Creator
Mohammadzadeh, Akbar , Akbaroghli, Susan , Aghaei-Moghadam, Ehsan , Mahdieh, Nejat , Badv, Reza Shervin , Jamali, Payman , Kariminejad, Roxana , Chavoshzadeh, Zahra , Ghasemi Firouzabadi, Saghar , Mansour Ghanaie, Roxana , Nozari, Ahoura , Banihashemi, Sussan , Hadipour, Fatemeh , Hadipour, Zahra , Kariminejad, Ariana , Najmabadi, Hossein , Shafeghati, Yousef and Behjati, Farkhondeh
Publisher
Iran: Royan Institute of Iran
Journal title
Language
English
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Publication information
Publisher
Iran: Royan Institute of Iran
Subjects
More information
Scope and Contents
Contents
Major birth defects are inborn structural or functional anomalies with long-term disability and adverse impacts on individuals, families, health-care systems, and societies. Approximately 20% of birth defects are due to chromosomal and genetic conditions. Inspired by the fact that neonatal deaths are caused by birth defects in about 20 and 10% of c...
Alternative Titles
Full title
Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian Patients with Multiple Congenital Anomalies
Authors, Artists and Contributors
Author / Creator
Akbaroghli, Susan
Aghaei-Moghadam, Ehsan
Mahdieh, Nejat
Badv, Reza Shervin
Jamali, Payman
Kariminejad, Roxana
Chavoshzadeh, Zahra
Ghasemi Firouzabadi, Saghar
Mansour Ghanaie, Roxana
Nozari, Ahoura
Banihashemi, Sussan
Hadipour, Fatemeh
Hadipour, Zahra
Kariminejad, Ariana
Najmabadi, Hossein
Shafeghati, Yousef
Behjati, Farkhondeh
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_doaj_primary_oai_doaj_org_article_7f76be7241904573b1cdae79e809ff61
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_7f76be7241904573b1cdae79e809ff61
Other Identifiers
ISSN
2228-5806
E-ISSN
2228-5814
DOI
10.22074/cellj.2019.6053
