𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Two patients with ring chromosome 15 syndrome

✍ Scribed by Butler, Merlin G. ;Fogo, Agnes B. ;Fuchs, David A. ;Collins, Francis S. ;Dev, Viathilingam G. ;Phillips, John A. ;Optiz, John M. ;Reynolds, James F.


Publisher
John Wiley and Sons
Year
1988
Tongue
English
Weight
387 KB
Volume
29
Category
Article
ISSN
0148-7299

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Ring chromosome 22 karyotype in a patien
✍ Christodoulou, John ;Bankier, Agnes ;Loughnan, Peter πŸ“‚ Article πŸ“… 1990 πŸ› John Wiley and Sons 🌐 English βš– 257 KB πŸ‘ 1 views

## To the Editor: The Opitz or BBBG syndrome is an autosomal dominant disorder characterized by facial anomalies and multiple congenital abnormalities. Recent evidence would suggest that the Opitz and BBB syndromes form a spectrum of the same condition Verloes et al., 19891 and it has been sugges

Chromosomal fragility in patients with t
✍ Reshmi-Skarja, Shalini ;Huebner, Angela ;Handschug, Katrin ;Finegold, David N. ; πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons 🌐 English βš– 109 KB πŸ‘ 2 views
Molecular and clinical characterization
✍ Gabriela Calounova; Petra Hedvicakova; Eva Silhanova; Gabriela Kreckova; Zdenek πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 English βš– 293 KB πŸ‘ 2 views

## Abstract Prader–Willi syndrome (PWS) is caused by the disturbed expression of genes from the imprinted region of 15q11‐q13, but the specific contributions of individual genes remain unknown. Most paternal PWS deletions are bracketed by recurrent breakpoints BP1 or BP2 and BP3. Atypical deletions