A Submicroscopic Deletion in Xq26 Associated with Familial Situs Ambiguus

Author:

Ferrero Giovanni B.,Gebbia Marinella,Pilia Giuseppe,Witte David,Peier Andrea,Hopkin Robert J.,Craigen William J.,Shaffer Lisa G.,Schlessinger David,Ballabio Andrea,Casey Brett

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference33 articles.

1. Sequence identification of 2,375 human brain genes;Adams;Nature,1992

2. Immotile-cilia syndrome (primary ciliary dyskinesia), including Kartagener syndrome;Afzelius,1994

3. Heterotaxia syndrome and autosomal dominant inheritance;Alonso;Am J Med Genet,1995

4. HNF-3β is essential for node and notochord formation in mouse development;Ang;Cell,1994

5. The spleen;Aylsworth,1993

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