Results 211 to 220 of about 179,204 (290)

Case Report: The nonsense variation of the cardiac transcription factor <i>NKX2-5</i> has been identified in a Chinese family with nonsyndromic congenital heart disease. [PDF]

Front Genet
Zhang H, Chen J, Wang H, Xiang Q, Liu S.
europepmc   +1 more source

Zero contrast technique in doubly committed subarterial ventricular septal defect closure in patient with body weight less than 10 kg: a case report. [PDF]

Front Cardiovasc Med
Prakoso R, Ariani R, Sembiring AA, Mendel B, Lilyasari O.   +4 more
europepmc   +1 more source

Tricuspid Atresia and Transposition of the Great Arteries in a Neonate With Successful Surgical Correction: A Case Report. [PDF]

Clin Case Rep
Borghol W, Karaja S, Takkem S.
europepmc   +1 more source

The Use of Multimodality Images in The Diagnosis of Unroofed Coronary Sinus Syndrome. [PDF]

JACC Case Rep
Ali M, Malik A, Bodker K, Ali A, Ghosoun N, Ajam T, Suma VS, Muthukumar L, Haddadian B, Jan MF, Galazka P, Tajik AJ.   +11 more
europepmc   +1 more source

Complementary role of echocardiography, karyotyping, and chromosomal microarray in congenital cardiac anomalies. [PDF]

Front Med (Lausanne)
Yin J, Zhang X, Wang Q, Cao Q, Ou H, Zhao Z, Xu S, Wang J, Xia L, Zhang B, Xiao X, Luo T, Wang X.   +12 more
europepmc   +1 more source

Pentalogy of Fallot: A case report. [PDF]

J Int Med Res
Zhong Z, Wen T.
europepmc   +1 more source

Dual-Phase Increase in Atrial Arrhythmia Prevalence Following Percutaneous Atrial Septal Defect Closure. [PDF]

J Soc Cardiovasc Angiogr Interv
Burke BJ, Goldar G, Rajeswaran J, Milinovich A, McCloskey O, Blazevic P, Saef J, Aziz PF, Karamlou T, Kanj M, Suntharos P, Marino BS, Komarlu R, Ghobrial J.   +13 more
europepmc   +1 more source

Mitral and tricuspid valve repair in an operated case of complete atrioventricular septal defect: A surgical challenge case report! [PDF]

SAGE Open Med Case Rep
Kumar D, Chandra A, Trehan N, Prakash S, Mehta Y, Mishra M, Bazaz S, Chandna S.   +7 more
europepmc   +1 more source

Application of chromosome microarray analysis and karyotyping in fetal cardiac abnormalities. [PDF]

Front Genet
Guo Y, Xin X, Zhou L, Huang J.
europepmc   +1 more source