𝔖 Bobbio Scriptorium
✦   LIBER   ✦

BBBG syndrome or opitz syndrome: New family

✍ Scribed by Verloes, Alain ;Le Merrer, Martine ;Briard, Marie-Louise


Publisher
John Wiley and Sons
Year
1989
Tongue
English
Weight
409 KB
Volume
34
Category
Article
ISSN
0148-7299

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Severe end of Opitz trigonocephaly (C) s
✍ Bohring, Axel; Silengo, Margherita; Lerone, Margherita; Superneau, Duane W.; Spa πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 83 KB πŸ‘ 3 views

We report on four unrelated cases of an Opitz trigonocephaly (C)-like syndrome with a highly characteristic combination of facial anomalies including prominent metopic suture, exophthalmos, hypertelorism, cleft lip and palate, flexion deformities of the upper limbs and multiple other anomalies. We a

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‘ 3 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