Omphalocele in trisomy 3q: further delineation of phenotype

Author:

Yatsenko SA,Mendoza-Londono R,Belmont JW,Shaffer LG

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference64 articles.

1. Further delineation of the dup(3q) syndrome;Wilson;Am J Med Genet,1985

2. The dup(3q) syndrome: report of eight cases and review of the literature;Steinbach;Am J Med Genet,1981

3. Chromosome 3 duplication q/deletion p syndrome;Fineman;Pediatrics,1978

4. Familial de Lange syndrome with chromosome abnormalities;Falek;Pediatrics,1966

5. Partial trisomy 3q and the mild Cornelia de Lange syndrome phenotype;Ireland;J Med Genet,1995

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