𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Identification and molecular characterization of the --CAMPANIA deletion, a novel α°-thalassemic defect, in two unrelated Italian families

✍ Scribed by Raffaele Sessa; Stella Puzone; Massimiliano Ammirabile; Carmelo Piscopo; Leonilde Pagano; Simona Colucci; Paola Izzo; Michela Grosso


Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
154 KB
Volume
85
Category
Article
ISSN
0361-8609

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Hb Q-Thailand-Hb H disease in a chinese
✍ P. Beris; P. Huber; P. A. Miescher; J. B. Wilson; A. Kutlar; S. S. Chen; Dr. T. 📂 Article 📅 1987 🏛 John Wiley and Sons 🌐 English ⚖ 402 KB 👁 1 views

Data on a 24-year-old Chinese male with Hb Q-Thailand-Hb H disease are presented. The hemoglobin variant was characterized by fast microprocedures, mainly by reverse-phase high-performance liquid chromatography. Gene mapping analyses identified the a-thalassemia-2, which is associated with the a-Q c

Molecular study of WISP3 in nine familie
✍ Valérie Delague; Eliane Chouery; Sandra Corbani; Ismat Ghanem; Suhail Aamar; Jud 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 299 KB 👁 2 views

## Abstract Progressive pseudorheumatoid dysplasia (PPD) is a rare autosomal recessive syndrome characterized by the presence of spondyloepiphyseal dysplasia associated with pain, stiffness, and swelling of multiple joints, osteoporosis, and the absence of destructive bone changes. The disorder is