𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Apparent Prader-Willi phenotype in a woman with ring chromosome 9

✍ Scribed by Hess, Russell O. ;Meisner, Lorraine F. ;Opitz, John M. ;Bernstein, Jay


Publisher
John Wiley and Sons
Year
1987
Tongue
English
Weight
362 KB
Volume
28
Category
Article
ISSN
0148-7299

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Prader-Willi syndrome phenotype in X chr
✍ Stratakis, Constantine A. πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 7 KB πŸ‘ 2 views

Recently, two female patients with supernumerary small marker X chromosome and a Prader-Willi syndrome (PWS)-like phenotype were reported by Tu Β¨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

Maternal isodisomy of chromosome 9 with
✍ BjοΏ½rck, Erik J.; Anderlid, Britt-Marie; Blennow, Elisabeth πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 22 KB πŸ‘ 2 views

We describe a 34-year-old healthy woman with isochromosomes for the short and long arm of chromosome 9 who was ascertained because of repeated spontaneous abortions. Molecular analysis demonstrated maternal uniparental isodisomy for the whole chromosome 9, thus the origin of the isochromosomes was m