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Results 1 - 10 of 82 for robert syndrome 11
  1. Cardiofaciocutaneous syndrome 
    ... a.31315. No abstract available. Citation on PubMed Roberts A, Allanson J, Jadico SK, Kavamura MI, Noonan J, Opitz JM, Young T, Neri G. The cardiofaciocutaneous syndrome. J Med Genet. 2006 Nov;43(11):833-42. doi: 10.1136/jmg.2006.042796. ...
    https://medlineplus.gov/.../condition/cardiofaciocutaneous-syndrome - Genetics
  2. Noonan syndrome 
    ... Zenker M, Zampino G, Verloes A, Dallapiccola B, Roberts AE, Cave H, Gelb BD, Neel BG, Tartaglia M. Activating Mutations Affecting the Dbl Homology Domain of SOS2 Cause Noonan Syndrome. Hum Mutat. 2015 Nov;36(11):1080-7. doi: 10.1002/humu.22834. Epub ...
    https://medlineplus.gov/genetics/condition/noonan-syndrome - Genetics
  3. Roberts syndrome 
    Roberts syndrome is a genetic disorder characterized by limb and facial abnormalities. Affected individuals also grow slowly before and after birth. Mild to ...
    https://medlineplus.gov/genetics/condition/roberts-syndrome - Genetics
  4. SMARCA4 gene 
    ... of the SWI/SNF complex cause Coffin-Siris syndrome. Nat Genet. 2012 Mar 18;44(4):376-8. doi: 10.1038/ng.2219. Citation on PubMed Wilson BG, Roberts CW. SWI/SNF nucleosome remodellers and cancer. Nat Rev Cancer. 2011 Jun 9;11(7):481-92. doi: 10.1038/nrc3068. Citation ...
    https://medlineplus.gov/genetics/gene/smarca4 - Genetics
  5. SMARCA2 gene 
    ... Azad AK, Mirshams M, Chen Z, Xu W, Roberts H, Shepherd FA, Tsao MS, Reisman D. ... International Consortium. Phenotype and genotype in Nicolaides-Baraitser ...
    https://medlineplus.gov/genetics/gene/smarca2 - Genetics
  6. ESCO2 gene 
    ... ESCO2 gene mutations have been found to cause Roberts syndrome, which is characterized by limb and facial abnormalities ... around the chromosome's constriction point (centromere). In Roberts syndrome, cells respond to abnormal sister chromatid attachment by ...
    https://medlineplus.gov/genetics/gene/esco2 - Genetics
  7. What Are the Symptoms of Down Syndrome? From the National Institutes of Health (Eunice Kennedy Shriver National Institute of Child Health and Human Development)  
    Down Syndrome/Symptoms ... Down Syndrome ... Eunice Kennedy Shriver National Institute of Child Health and Human Development ... From the National Institutes of Health
    https://www.nichd.nih.gov/health/topics/down/conditioninfo/symptoms - External Health Links
  8. PTPN11 gene 
    ... adolescents. More About This Health Condition At least 11 mutations in the PTPN11 gene have been found ... time. BPTP3 protein tyrosine phosphatase, non-receptor type 11 (Noonan syndrome 1) protein-tyrosine phosphatase 2C PTN11_ ...
    https://medlineplus.gov/genetics/gene/ptpn11 - Genetics
  9. PRKAG2 gene 
    ... on PubMed Gollob MH, Green MS, Tang AS, Roberts R. PRKAG2 cardiac syndrome: familial ventricular preexcitation, conduction system disease, and cardiac ...
    https://medlineplus.gov/genetics/gene/prkag2 - Genetics
  10. National Institute of Environmental Health Sciences (National Institute of Environmental Health Sciences)  
    ... 07 NIEHS-08 NIEHS-09 NIEHS-10 NIEHS-11 Translational Toxicology Division Strategic Research Framework Exposure-Based ... Studying Environmental Connections Between Diet and Disease October 11 - Connecting DNA, Autoimmunity, and the Environment September 19, ...
    https://www.niehs.nih.gov - Other Resources
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