Deletion Within Chromosome 22 is Common in Patients With Absent Pulmonary Valve Syndrome
- 31 July 1995
- journal article
- Published by Elsevier in The American Journal of Cardiology
- Vol. 76 (1-2) , 66-69
- https://doi.org/10.1016/s0002-9149(99)80803-0
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.Journal of Medical Genetics, 1993
- DiGeorge syndrome: part of CATCH 22.Journal of Medical Genetics, 1993
- Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects.Journal of Medical Genetics, 1993
- Routine diagnosis of DiGeorge syndrome by fluorescent in situ hybridizationHuman Genetics, 1993
- Velo‐cardio‐facial syndrome: A review of 120 patientsAmerican Journal of Medical Genetics, 1993
- Deletions and microdeletions of 22q11.2 in velo‐cardio‐facial syndromeAmerican Journal of Medical Genetics, 1992
- Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locusThe Lancet, 1992
- Cardiovascular anomalies in digeorge syndrome and importance of neural crest as a possible pathogenetic factorPublished by Elsevier ,1986
- Tetralogy of Fallot with absent pulmonic valve: analysis of 17 patientsThe American Journal of Cardiology, 1984
- Inhibitory effect of ethidium bromide on mitotic chromosome condensation and its application to high-resolution chromosome bandingCytogenetic and Genome Research, 1984