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The Coffin syndrome (1977)

Fryns, J. P. ; Vinken, L. ; Berghe, H.

Springer

Human genetics 〈Berlin〉 36 (1977), S. 271-276

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ISSN: 1432-1203

Source: Springer Online Journal Archives 1860-2000

Topics: Biology , Medicine

Notes: Summary Two brothers with Coffin syndrome are presented and the fifteen other cases available in the literature are reviewed. The molecular defect causing this clinically recognizable syndrome is unknown, and the mode of inheritance may be a sex-linked recessive, but a sex-limited autosomal dominant or autosomal dominant with variable degree of expression cannot be fully excluded at the present time.

Type of Medium: Electronic Resource

URL: http://dx.doi.org/10.1007/BF00446276

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