Further comments on the lissencephaly syndromes.

W. B. Dobyns, E. F. Gilbert, J. M. Opitz

Research output: Contribution to journalReview articlepeer-review

27 Scopus citations

Abstract

Detailed clinical, pathological, and cytogenetic investigations of patients with lissencephaly over the past several years have demonstrated the existence of at least eight distinct conditions with variable genetic implications. In several of these disorders, especially chromosomally normal MDS, ILS, and CCL, too few patients have been reported to permit citation of accurate recurrence risk figures. Accordingly, we wish to begin a registry of patients with lissencephaly of all types for the purpose of developing such risk figures and request that any available information be sent to one of us (W.B.D. or J.M.O.).

Original languageEnglish (US)
Pages (from-to)197-211
Number of pages15
JournalAmerican Journal of Medical Genetics
Volume22
Issue number1
DOIs
StatePublished - Sep 1985
Externally publishedYes

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