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Chromosome 22q11 microdeletion and congenital heart disease – a survey in a paediatric population

✍ Scribed by D. E. J. Yong; P. Booth; J. Baruni; D. Massie; G. Stephen; D. Couzin; J. C. S. Dean

Book ID
106122930
Publisher
Springer
Year
1999
Tongue
English
Weight
70 KB
Volume
158
Category
Article
ISSN
0340-6997

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22q11 microdeletion studies in the heart
22q11 microdeletion studies in the heart tissue of an abortus involving a familial form of congenital heart disease
✍ Z.M. Patel; H.M. Gawde; M.I. Khatkhatay 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 169 KB

## Abstract Microdeletion of chromosome 22 is responsible for DiGeorge syndrome, Velo Cardio Facial syndrome, and conotruncal defects. Here, we report on a case of microdeletion 22q11.2 in the heart tissue of a miscarried fetus in a family whose two children had died due to complex congenital heart