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Long survival in a 69,XXY triploid male

✍ Scribed by Sherard, J. ;Bean, Charles ;Bove, Betsy ;DelDuca, Vincent ;Esterly, K. L. ;Karcsh, Henry J. ;Munshi, Gaurang ;Reamer, James F. ;Suazo, Gloria ;Wilmoth, Donna ;Dahlke, Mariam B. ;Weiss, Carol ;Borgaonkar, Digamber S. ;Reynolds, James F.


Publisher
John Wiley and Sons
Year
1986
Tongue
English
Weight
465 KB
Volume
25
Category
Article
ISSN
0148-7299

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## Abstract The 18q‐ syndrome is relatively common among cytogenetic abnormalities occurring in approximately 1 in 40,000 live births. However, interstitial deletions involving 18q12.2 to q21.1 are much less common. Only 15 cases have been reported in the literature. A phenotypic pattern is emergin