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Results 1 - 10 of 290 for Four X syndrome
  1. 49,XXXXY syndrome 
    ... Y chromosome (46,XY). People with 49,XXXXY syndrome have a single Y chromosome and four copies of the X chromosome, for a total of 49 chromosomes in each cell.Individuals with 49,XXXXY syndrome have extra copies of multiple genes on the ...
    https://medlineplus.gov/genetics/condition/49xxxxy-syndrome - Genetics
  2. TNXB gene 
    ... MM. Well-defined clinical presentation of Ehlers-Danlos syndrome in patients with tenascin-X deficiency: a report of four cases. Clin Dysmorphol. 2012 Jan;21(1):15- ...
    https://medlineplus.gov/genetics/gene/tnxb - Genetics
  3. X chromosome 
    ... physical features, and infertility. Individuals with 49,XXXXY syndrome have the usual single Y chromosome plus four copies of the X chromosome, for a total of 49 chromosomes in ...
    https://medlineplus.gov/genetics/chromosome/x - Genetics
  4. Fragile X-Associated Disorders (FXD): A Handbook for Families, Health Care Providers, Counselors, and Educators (National Fragile X Foundation) - PDF  
    Fragile X Syndrome/Start Here ... Fragile X Syndrome ... National Fragile X Foundation ... PDF ... fragile x, handbook, 3rd edition, NFXF
    https://fragilex.org/.../2012/01/Handbook-FXD_3rd_Edition.pdf - External Health Links
  5. Brain Facts: Glossary (Society for Neuroscience)  
    Brain Diseases/Reference Desk ... Brain Diseases ... Society for Neuroscience
    https://www.brainfacts.org/Glossary - External Health Links
  6. Griscelli syndrome 
    ... N, de Saint Basile G, Sanal O. Griscelli syndrome types 1 and 3: analysis of four new cases and long-term evaluation of previously diagnosed patients. Eur J Pediatr. 2012 Oct;171(10):1527-31. doi: 10.1007/s00431-012-1765-x. Epub 2012 Jun 19. Citation on PubMed Menasche ...
    https://medlineplus.gov/genetics/condition/griscelli-syndrome - Genetics
  7. PPM-X syndrome 
    ... Fryssira-Kanioura H. Phenotypic and genotypic variability in four males with MECP2 gene ... or Free article on PubMed Central
    https://medlineplus.gov/genetics/condition/ppm-x-syndrome - Genetics
  8. FHL1 gene 
    ... been found in people with reducing body myopathy, X-linked scapuloperoneal myopathy, and rigid spine syndrome, but it is unclear how they are related to the major features of these disorders. bA535K18.1 FHL-1 FHL1A FHL1B FLH1A four-and-a-half Lin11, Isl-1 and Mec- ...
    https://medlineplus.gov/genetics/gene/fhl1 - Genetics
  9. Tourette Syndrome: A Not-So-Frightening Diagnosis (American Academy of Pediatrics)  
    Tourette Syndrome/Children ... Tourette Syndrome ... Movement Disorders/Children ... Movement Disorders ... American Academy of Pediatrics
    https://www.healthychildren.org/...cs-Tourette-Syndrome-and-OCD.aspx - External Health Links
  10. MT-TL1 gene 
    ... doi: 10.1111/j.1464-5491.2008.02359.x. Epub 2008 Feb 18. Citation on PubMed Opdal SH, Rognum TO, Torgersen H, Vege A. Mitochondrial DNA point mutations detected in four cases of sudden infant death syndrome. Acta Paediatr. 1999 Sep;88(9):957-60. ...
    https://medlineplus.gov/genetics/gene/mt-tl1 - Genetics
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