6p.24 microdeletion involvingTFAP2Awithout classic features of branchio-oculo-facial syndrome

Author:

LeBlanc Shannon K.,Yu Sui,Barnett Christopher P.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference19 articles.

1. A novel TFAP2A mutation in familial branchio-oculo-facial syndrome with predominant ocular phenotype;Aliferis;Ophthalmic Genet,2011

2. An interstitial deletion of 6p24-p25 proximal to the FKHL7 locus and including AP-2α that affects anterior eye chamber development;Davies;J Med Genet,1999a

3. Delineation of two distinct 6p deletion syndromes;Davies;Hum Genet,1999b

4. Recurrence of orbital cysts in the branchio-oculo-facial syndrome;Fielding;J Med Genet,1992

5. New autosomal dominant branchio-oculo-facial syndrome;Fujimoto;Am J Med Genet,1987

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