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Results 1 - 10 of 13 for Monosomy X
  1. ... About half of individuals with Turner syndrome have monosomy X, which means each cell in the individual's ... not inherited. When this condition is caused by monosomy X, the chromosomal abnormality occurs as a random event ...
  2. ... cell is sufficient to cause the disorder. Familial Turner syndrome Female pseudo-Turner syndrome Male Turner syndrome Noonan's syndrome Noonan-Ehmke syndrome NS Pseudo- ...
  3. ... BM, Hoskote SS, Spinner RJ, Klein CJ. Parsonage-Turner Syndrome and Hereditary Brachial Plexus Neuropathy. Mayo Clin Proc. ...
  4. ... childhood: contrasting children with Leri-Weill dyschondrosteosis and Turner syndrome. J Pediatr. 2005 Oct;147(4):499-507. ...
  5. ... of these genetic conditions, such as Down syndrome, Turner syndrome, and 22q11.2 deletion syndrome, result from changes ...
  6. ... material in 47,XXX syndrome-A comparison with Turner syndrome and 46,XX females. Am J Med Genet ...
  7. ... E, Lennarts M, Janssen JW, Engelen JJ. Partial monosomy 8p/trisomy 8q in a newborn infant due ... Citation on PubMed
  8. ... disorder Jacobsen thrombocytopenia ... syndrome). Neurogenetics. 2009 Apr;10(2):89-95. doi: 10.1007/s10048-008-0157-x. Epub 2008 Oct 15. Citation on PubMed or ...
  9. ... deletion syndrome Distal deletion 10q Distal monosomy 10q Monosomy 10qter Telomeric deletion 10 Terminal chromosome ... Epub 2009 Jun 22. Citation on PubMed
  10. ... deletion Microdeletion 9q22.3 syndrome ... Citation on PubMed Yamamoto K, Yoshihashi H, Furuya ...
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