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Hemihypertrophy with hypomelanosis of Ito: A new syndrome combination

Goswami HK

  • KMID: 1538076
  • J Genet Med.
  • 1998 Mar;2(1):1-6.
A female hemihypertrophy patient with hypomelanosis of Ito is presented as a rare case combining classical features of both the syndrome. Chromosomal profile has been based on longitudinal study of...
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Unusual chromosomal features in a child with gradual disappearance of right ulna (mono ostolic osteolysis)

Goswami HK, Shrivastava N, Gopal SK, Sharna S, Chandorkar M, Lee IH, Chang SK

  • KMID: 1963058
  • J Genet Med.
  • 1997 Sep;1(1):11-16.
A nine month old male child presenting degenerating right ulna (massive osteolysis) has been followed up for two years. The bone completely disappeared due to abscesses on the right forearm...
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