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. 1983 Jun 4;1(8336):1285-6.
doi: 10.1016/s0140-6736(83)92745-9.

Parental origin of chromosome 15 deletion in Prader-Willi syndrome

M G Butler, C G Palmer

Parental origin of chromosome 15 deletion in Prader-Willi syndrome

M G Butler et al. Lancet. .
No abstract available

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References

    1. Prader A, Labhart A, Willi H. Ein Syndrom von Adipositas, Kleinwuch, Kryptorchismus and Oligophrenic nach Myatonieratigam Zustad in Neugeborcnenalter. Schweiz Med Wischr. 1956;86:1260–61.
    1. Zellweger H, Schneider HJ. Syndromes of hypotonia, hypornentia- hypogonadism – obesity (HHHO) or Prader-Willi syndrome. Am J Dis Child. 1968;115:588–98. - PubMed
    1. Hall BD, Smith DW. Prader-Willi syndrome. J Pediatr. 1972;52:286–93. - PubMed
    1. Ledbetter DH, Riccardi VM, Airhart SD, Strobel RJ, Kennan BS, Crawford JD. Deletions of chromosome 15 as a cause of the Prader-Willi syndrome. N Engl J Med. 1981;304:325–29. - PubMed
    1. Butler MG, Meaney FJ, Kaler SG, Yu PL, Palmer CG. Clinical differences between chromosome 15q deletion and nondeletion Prader-Willi individuals. Am J Hum Genet. 1982;34:119A.

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