Literature DB >> 24214527

Trisomy 13 (Patau syndrome) and congenital heart defects.

Janaina B Polli1, Daniela de P Groff, Patrícia Petry, Vinícius F Mattos, Rosana C M Rosa, Paulo R G Zen, Carla Graziadio, Giorgio A Paskulin, Rafael F M Rosa.   

Abstract

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Year:  2013        PMID： 24214527     DOI： 10.1002/ajmg.a.36193

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN： 1552-4825            Impact factor:   2.802


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  5 in total

Review 1.  Cytogenomic Aberrations in Congenital Cardiovascular Malformations.

Authors:  Mahshid Azamian; Seema R Lalani
Journal:  Mol Syndromol       Date:  2016-04-26

2.  Role of Overexpressed Transcription Factor FOXO1 in Fatal Cardiovascular Septal Defects in Patau Syndrome: Molecular and Therapeutic Strategies.

Authors:  Adel Abuzenadah; Saad Al-Saedi; Sajjad Karim; Mohammed Al-Qahtani
Journal:  Int J Mol Sci       Date:  2018-11-10       Impact factor: 5.923

3.  An infant with patau syndrome associated with congenital heart defects.

Authors:  Ubaid Khan; Ahmad Hussain; Muhammad Usman; Zain Ul Abiddin
Journal:  Ann Med Surg (Lond)       Date:  2022-07-02

4.  Association of GDF1 rs4808863 with fetal congenital heart defects: a case-control study.

Authors:  Juan Zhang; Qingqing Wu; Li Wang; Xiaofei Li; Yuqing Ma; Ling Yao
Journal:  BMJ Open       Date:  2015-12-11       Impact factor: 2.692

5.  The Prevalence of Congenital Heart Diseases in Syndromic Children at King Khalid National Guard Hospital from 2005 to 2016.

Authors:  Elaf M Abduljawad; Ahad AlHarthi; Samah A AlMatrafi; Mawaddah Hussain; Aiman Shawli; Rahaf Waggass
Journal:  Cureus       Date:  2020-04-29
  5 in total

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