Publisher
Springer Science and Business Media LLC
Reference30 articles.
1. Sanjad, S.A., Sakati, N.A., Abu-Osba, Y.K., Kaddoura, R. & Milner, R.D. A new syndrome of congenital hypoparathyroidism, severe growth failure, and dysmorphic features. Arch. Dis. Child. 66, 193–196 (1991).
2. Richardson, R.J. & Kirk, J.M. Short stature, mental retardation, and hypoparathyroidism: a new syndrome. Arch. Dis. Child. 65, 1113–1117 (1990).
3. Hershkovitz, E. et al. The new syndrome of congenital hypoparathyroidism associated with dysmorphism, growth retardation, and developmental delay—a report of six patients. Isr. J. Med. Sci. 31, 293–297 (1995).
4. Khan, T.S.K. et al. Kenny–Caffey syndrome in six Bedouin sibships: autosomal recessive inheritance is confirmed. Am. J. Med. Genet. 69, 126–132 (1997).
5. Parvari, R. et al. Homozygosity and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM interval on chromosome 1q42-43. Am. J. Hum. Genet. 63, 163–169 (1998).
Cited by
224 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献