Associated Papers
Characterization of the chromosome 1q41q42.12 region, and the candidate gene DISP1, in patients with CDH.
Kantarci S et al.
American Journal of Medical Genetics. Part A, 2010
Exome sequencing identifies ZFPM2 as a cause of familial isolated congenital diaphragmatic hernia and possibly cardiovascular malformations.
Brady PD et al.
European Journal of Medical Genetics, 0
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