Brief clinical report: A genetic association between microcephaly and lymphedema
Identifieur interne : 003F83 ( Istex/Curation ); précédent : 003F82; suivant : 003F84Brief clinical report: A genetic association between microcephaly and lymphedema
Auteurs : Carol A. Crowe [États-Unis] ; Lois H. Dickerman [États-Unis] ; John M. Opitz [États-Unis] ; James F. Reynolds [États-Unis]Source :
- American Journal of Medical Genetics [ 0148-7299 ] ; 1986-05.
Abstract
We discuss a family in which microcephaly and lymphedema are co‐segregating as an apparently autosomal or X‐linked dominant trait. A review of each malformation is presented with reference to the known genetic patterns of each. This combination of microcephaly and lymphedema may be a unique syndrome, previously undescribed because of subtleties of expression in affected individuals.
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DOI: 10.1002/ajmg.1320240116
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A review of each malformation is presented with reference to the known genetic patterns of each. This combination of microcephaly and lymphedema may be a unique syndrome, previously undescribed because of subtleties of expression in affected individuals.</div></front></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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