New hereditary malformation syndrome of unusual facial appearance, skeletal deformities, and musculoskeletal and sensory defects

Author:

Middleton L. T.,Anastasiades V.,Panayidou K.,Georghiou D.,Kalli E.,Gabriel G.,Myrianthopoulos N. C.

Publisher

Wiley

Subject

Genetics(clinical)

Reference10 articles.

1. Familial Osteodysplasia

2. (1986): Congenital deformities. In (eds): “Myology.” New York: McGraw-Hill, pp 2109-2159.

3. (1989): Unusual facies, cataract, short stature, joint abnormalities and spondyloepimetaphyseal dysplasia in sibs. A new premature aging-like autosomal syndrome? David W. Smith Workshop on Malformations and Morphogenesis, Madrid, Spain.

4. The median cleft face syndrome: Differential diagnosis of cranium bifidum occultum, hypertelorism, and median cleft nose, lip, and palate

5. (1990): “Syndromes of the Head and the Neck.” New York: Oxford University Press, 3rd ed.

Cited by 2 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

1. Arthrogryposes (Multiple Congenital Contractures);Emery and Rimoin's Principles and Practice of Medical Genetics;2013

2. REFERENCES (GAMUTS);Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007

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