OEIS complex associated with chromosome 1p36 deletion: A case report and review

Author:

El-Hattab Ayman W.,Skorupski Josh C.,Hsieh Michael H.,Breman Amy M,Patel Ankita,Cheung Sau Wai,Craigen William J.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference52 articles.

1. Further delineation of deletion 1p36 syndrome in 60 patients: A recognizable phenotype and common cause of developmental delay and mental retardation;Battaglia;Pediatrics,2008

2. OEIS complex: Prenatal ultrasound and autopsy findings;Ben-Neriah;Ultrasound Obstet Gynecol,2007

3. Wnt induces LRP6 signalosomes and promotes dishevelled-dependent LRP6 phosphorylation;Bilic;Science,2007

4. Large rearrangements detected by MLPA, point mutations, and survey of the frequency of mutations within the SLC3A1 and SLC7A9 genes in a cohort of 172 cystinuric Italian patients;Bisceglia;Mol Genet Metab,2009

5. OEIS complex, VATER, and the ongoing difficulties in terminology and delineation (Letter);Bohring;Am J Med Genet,2002

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