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Case Reports
. 1989 May;26(5):337-9.
doi: 10.1136/jmg.26.5.337.

Synchrony of oculocutaneous albinism, the Prader-Willi syndrome, and a normal karyotype

C E Wallis  1 , P H Beighton
Affiliations
Case Reports

Synchrony of oculocutaneous albinism, the Prader-Willi syndrome, and a normal karyotype

C E Wallis et al. J Med Genet. 1989 May.

Abstract

A Chinese girl with oculocutaneous albinism has the Prader-Willi syndrome and a normal karyotype. This association emphasises the importance of further molecular study of the 15(q12) region of the genome in the search for the locus of an albinism gene.

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References

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