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Published in

Wiley, American Journal of Medical Genetics, 2(66), p. 221-226

DOI: 10.1002/(sici)1096-8628(19961211)66:2<221::aid-ajmg19>3.0.co;2-v

Wiley, American Journal of Medical Genetics, 2(66), p. 221-226

DOI: 10.1002/(sici)1096-8628(19961211)66:2<221::aid-ajmg19>3.3.co;2-1

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Phenotypic differences in Angelman syndrome patients: Imprinting mutations show less frequently microcephaly and hypopigmentation than deletions

Journal article published in 1996 by Joachim Bürger, Jürgen Kunze, Karl Sperling, André Reis ORCID
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

Full text: Unavailable

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Preprint: archiving allowed
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Postprint: archiving restricted
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Published version: archiving forbidden
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