✦ LIBER ✦
Prader-Willi-like phenotype: investigation of 1p36 deletion in 41 patients with delayed psychomotor development, hypotonia, obesity and/or hyperphagia, learning disabilities and behavioral problems
✍ Scribed by Carla S. D'Angelo; José A. Da Paz; Chong A. Kim; Débora R. Bertola; Claudia I.E. Castro; Monica C. Varela; Célia P. Koiffmann
- Book ID
- 116432984
- Publisher
- Elsevier Science
- Year
- 2006
- Tongue
- English
- Weight
- 522 KB
- Volume
- 49
- Category
- Article
- ISSN
- 1769-7212
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