Holt-Oram Sendromlu Hastada Primum Tip Atriyal Septal Defekt ve Patent Foramen Ovale Birlikteliği
Year 2019,
Volume: 22 Issue: 2, 141 - 142, 15.08.2019
Hasan Kaya
,
Mehmet Sait Coşkun
Celal Yavuz
Faruk Ertaş
References
- 1. Basson CT, Cowley GS, Solomon SD, Weissman B, Poznanski AK, Traill TA, et al. The clinical and genetic spectrum of the Holt-Oram syndrome (Heart-Hand syndrome). N Engl J Med 1994;330:885-91.
- 2. Çakır Ö, Eren MN, Kesemenli C. HOLT-ORAM SYNDROME (Heart-Hand Syndrome): Case Report. Turk Gogus Kalp Dama 2002;10:247-8.
- 3. Holt M, Oram S. Familial heart disease with skeletal malformations. Br Heart J 1960;22:236-42.
Association of Primum-Type Atrial Septal Defect and Patent Foramen Ovale in a Patient with Holt-Oram Syndrome
Year 2019,
Volume: 22 Issue: 2, 141 - 142, 15.08.2019
Hasan Kaya
,
Mehmet Sait Coşkun
Celal Yavuz
Faruk Ertaş
References
- 1. Basson CT, Cowley GS, Solomon SD, Weissman B, Poznanski AK, Traill TA, et al. The clinical and genetic spectrum of the Holt-Oram syndrome (Heart-Hand syndrome). N Engl J Med 1994;330:885-91.
- 2. Çakır Ö, Eren MN, Kesemenli C. HOLT-ORAM SYNDROME (Heart-Hand Syndrome): Case Report. Turk Gogus Kalp Dama 2002;10:247-8.
- 3. Holt M, Oram S. Familial heart disease with skeletal malformations. Br Heart J 1960;22:236-42.
There are 3 citations in total.