CCBE1 mutations can cause a mild, atypical form of generalized lymphatic dysplasia but are not a common cause of non‐immune hydrops fetalis
- 12 January 2012
- journal article
- Published by Wiley in Clinical Genetics
- Vol. 81 (2), 191-197
- https://doi.org/10.1111/j.1399-0004.2011.01731.x
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
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- Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasiaHuman Genetics, 2009
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- ccbe1 is required for embryonic lymphangiogenesis and venous sproutingNature Genetics, 2009
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- Severity of Non-Immune Hydrops Fetalis at Birth Continues to Predict Survival despite Advances in Perinatal CareFetal Diagnosis and Therapy, 2006
- Autosomal recessive intestinal lymphangiectasia and lymphedema, with facial anomalies and mental retardationAmerican Journal of Medical Genetics, 1989
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