✦ LIBER ✦

Brachyolmia with amelogenesis imperfecta: Further evidence of a distinct entity

✍ Scribed by D.R. Bertola; R. Antequera; M.J. Rodovalho; R.S. Honjo; L.M.J. Albano; I.M. Furquim; L.A. Oliveira; C.A. Kim

Book ID: 101450116
Publisher: John Wiley and Sons
Year: 2009
Tongue: English
Weight: 108 KB
Volume: 149A
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.32661

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Upper respiratory tract carcinoma with c

Upper respiratory tract carcinoma with chromosomal translocation 15;19 : Evidence for a distinct disease entity of young patients with a rapidly fatal course

✍ Sara O. Vargas; Christopher A. French; Peter N. Faul; Jonathan A. Fletcher; Ian 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 496 KB 👁 1 views

Genetic polymorphism of a haemoglobin ch

Genetic polymorphism of a haemoglobin chain and adenosine deaminase in European shads: evidence for the existence of two distinct genetic entities with natural hybridization

✍ P. J. Alexandrino; N. Ferrand; J. Rocha 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 557 KB

Retinitis pigmentosa in a young man with

Retinitis pigmentosa in a young man with Noonan syndrome: Further evidence that Noonan syndrome (NS) and the cardio-facio-cutaneous syndrome (CFC) are variable manifestations of the same entity?

✍ Lorenzetti, Maria-Elena; Fryns, Jean-Pierre 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 285 KB 👁 2 views

W e report on a young man with Noonan syndrome (NS) and retinitis pigmentosa. As far as we know, retinitis pigmentosa has not been reported in NS. However, in the 3 cardio-facio-cutaneous syndrome (CFC) patients in whom electroretinographic studies were performed, retinal anomalies have been found.