## Abstract The chromosome 9q subtelomere deletion syndrome (9qSTDS) is among the first and most common clinically recognizable syndromes to arise from widespread testing by fluorescent in situ hybridization (FISH) of subtelomere deletions. There are about 50 reported cases worldwide. Affected indi
✦ LIBER ✦
Subtelomeric deletions of chromosome 9q: A novel microdeletion syndrome
✍ Scribed by Douglas R. Stewart; Alina Huang; Francesca Faravelli; Britt-Marie Anderlid; Livija Medne; Karen Ciprero; Maninder Kaur; Elena Rossi; Romano Tenconi; Magnus Nordenskjöld; Karen W. Gripp; Linda Nicholson; Wendy S. Meschino; Esther Capua; Oliver W.J. Quarrell; Jonathon Flint; Mira Irons; Philip F. Giampietro; David B. Schowalter; Christina A. Zaleski; Michela Malacarne; Elaine H. Zackai; Nancy B. Spinner; Ian D. Krantz
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 319 KB
- Volume
- 128A
- Category
- Article
- ISSN
- 1552-4825
No coin nor oath required. For personal study only.
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