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Results 1 - 10 of 17 for Lymphatic malformation 4
  1. ... Am J Med Genet. 2002 Nov 1;112(4):412-21. doi: 10.1002/ajmg.10707. Citation on PubMed
  2. ... Organization for Rare Disorders (NORD) ClinicalTrials.gov ... dysplasia: an update from 2010 to include molecular findings. Clin Genet. 2013 Oct;84(4):303-14. doi: 10.1111/cge.12173. Epub ...
  3. Lymphedema (Lymphatic Education & Research Network)  
    Lymphedema/Start Here ... Lymphedema ... Lymphatic Education & Research Network ... lymphedema, lymphatic system, risk of lymphedema, treatment for lymphedema ... Lymphedema ...
  4. ... National Organization for Rare Disorders (NORD) ClinicalTrials.gov LYMPHATIC MALFORMATION 1; LMPHM1 PubMed Brice G, Child AH, Evans ... and atypical presentations. Clin Genet. 2006 Oct;70(4):330-5. doi: 10.1111/j.1399-0004. ...
  5. ... GJC2 PubMed GAP JUNCTION PROTEIN, GAMMA-2; GJC2 LYMPHATIC MALFORMATION 3; LMPHM3 SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE; SPG44 ... doi: 10.1093/brain/awn328. Epub 2008 Dec 4. Citation on PubMed or Free article on PubMed ...
  6. How Do Health Care Providers Diagnose Congenital Anomalies? Easy-to-Read From the National Institutes of Health (Eunice Kennedy Shriver National Institute of Child Health and Human Development)  
    Birth Defects/Diagnosis and Tests ... Birth Defects ... Eunice Kennedy Shriver National Institute of Child Health and Human Development ... Easy-to-Read ... From the National ...
  7. ... birth. More About This Health Condition AOS6 delta 4 delta ligand 4 delta-like 4 (Drosophila) delta-like 4 homolog ...
  8. ... alpha phosphatidylinositol 3-kinase, catalytic, alpha polypeptide phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform phosphatidylinositol-4,5-bisphosphate 3-kinase 110 kDa catalytic subunit ...
  9. ... cause Hennekam syndrome, an inherited disorder resulting from malformation of the lymphatic system, which consists of a network of vessels ... member 11 CDHF14 CDHR11 FAT tumor suppressor homolog 4 FAT-J fat-like cadherin protein FAT-J ...
  10. ... cause Hennekam syndrome, an inherited disorder resulting from malformation of the lymphatic system. Most CCBE1 gene mutations change single protein ... humans. Nat Genet. 2009 Dec;41(12):1272-4. doi: 10.1038/ng.484. Citation on PubMed ...
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