Seckel syndrome is a rare, recessively inherited disorder of severe growth retardation and distinct craniofacial, orodental, and skeletal anomalies. Even though there are well-established minimum diagnostic criteria for this syndrome, controversy exists about its boundaries and criteria for exclusio
✦ LIBER ✦
Moyamoya-like vasculopathy and Seckel syndrome: just a coincidence?
✍ Scribed by Ralph Rahme; Louis Crevier; Josée Dubois; Claude Mercier
- Book ID
- 106052952
- Publisher
- Springer
- Year
- 2010
- Tongue
- English
- Weight
- 285 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0256-7040
No coin nor oath required. For personal study only.
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