✦ LIBER ✦
A search for chromosome 22q11.2 deletions in a series of 176 consecutively catheterized patients with congenital heart disease: no evidence for deletions in non-syndromic patients
✍ Scribed by S. Borgmann; I. Luhmer; M. Arslan-Kirchner; H. -C. Kallfelz; J. Schmidtke
- Book ID
- 106122990
- Publisher
- Springer
- Year
- 1999
- Tongue
- English
- Weight
- 86 KB
- Volume
- 158
- Category
- Article
- ISSN
- 0340-6997
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