Long QT syndrome associated with syndactyly identified in females
The identification of female children with this syndrome is evidence that this disorder is not X-linked in inheritance. Possible inheritance modes still include autosomal recessive or, more likely, a de novo mutation, given the absence of family history in any of the patients. Children of both sexes...
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Veröffentlicht in: | The American journal of cardiology 1995-10, Vol.76 (10), p.744-745 |
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Sprache: | eng |
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