Recently, two female patients with supernumerary small marker X chromosome and a Prader-Willi syndrome (PWS)-like phenotype were reported by Tu ¨mer et al. [1998]. Both patients presented during childhood with obesity that started around the third year of life, mental retardation, small hands and fe
Preliminary evidence for a cognitive phenotype in Barth syndrome
✍ Scribed by Mazzocco, Mich�le M.M. ;Kelley, Richard I.
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 91 KB
- Volume
- 102
- Category
- Article
- ISSN
- 0148-7299
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