Familial occurrence of a syndrome with mental retardation, nasal hypoplasia, peripheral dysostosis, and blue eyes in Japanese siblings-Reference-Cited by-同舟云学术

Familial occurrence of a syndrome with mental retardation, nasal hypoplasia, peripheral dysostosis, and blue eyes in Japanese siblings

Published:1978 Issue:2 Volume:42 Page:227-232
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Niikawa N.,Matsuda I.,Ohsawa T.,Kajii T.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00283643.pdf

Reference4 articles.

1. Giedion, A.: Acrodysplasia. Cone-shaped epiphyses, peripheral dysostosis, Thieman's disease and acrodysostosis. Prog. Pediatr. Radiol. 4, 325?345 (1973)

2. Jones, K. L., Smith, D. W., Harvey, M. A. S., Hall, B. D., Quan, L.: Older paternal age and fresh gene mutation: Data and additional disorders. J. Pediatr. 86, 84?88 (1975)

3. Rimoin, D. L., Hollister, D. W.: Acrodysostosis. In: Birth Defects Atlas and Compendium, D. Bergsma, ed. The National Foundation March of Dimes. Baltimore: Williams and Wilkins Co. 1973

4. Robinow, M., Pfeiffer, R. A., Gorlin, R. J., McKusick, V. A., Renuart, A. W., Johnson, G. F., Summitt, R. L.: Acrodysostosis. A syndrome of peripheral dysostosis, nasal hypoplasia, and mental retardation. Am. J. Dis. Child. 121, 195?203 (1971)

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