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Clinical characteristics of children with hypoparathyroidism due to 22q11.2 microdeletion

✍ Scribed by M. Adachi; K. Tachibana; M. Masuno; Y. Makita; H. Maesaka; T. Okada; K. Hizukuri; K. Imaizumi; Y. Kuroki; H. Kurahashi; S. Suwa


Publisher
Springer
Year
1998
Tongue
English
Weight
226 KB
Volume
157
Category
Article
ISSN
0340-6997

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Laryngeal atresia type III (glottic web)
✍ Fokstuen, Siv; Bottani, Armand; Medeiros, Paula F. V.; Antonarakis, Stylianos E. πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 394 KB πŸ‘ 1 views

The clinical manifestations of patients with a 22q11.2 deletion are highly variable and mainly include developmental defects of structures derived from the third and fourth pharyngeal pouches. Laryngeal atresia has occasionally been reported in Di-George syndrome as well as in velo-cardiofacial synd