[Marshall syndrome: Clinical, radiological and genetical features of a Tunisian family].

Rania Sakka,Emna Kerkeni,Myriam Chaabouni, Fatma Zohra Chioukh, Sofiène Ben Amor, Ridha M'rad, Salim Ben Yahia,Habiba Chaabouni,Kamel Monastiri

La Tunisie medicale（2015）

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摘要

There is a variability of the clinical expression among the affected members of the study's family. We will continue searching the causative mutation to establish a clear genotype- phenotype correlation.

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