Familial oculo-cutaneous hypopigmentation of dominant transmission due to a disorder in melanocyte formation. Association of Prader-Willi syndrome with a chromosome abnormality in one of the subjects involved (Q41349292)
scientific article published on December 31, 1977
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Current Data About Familial oculo-cutaneous hypopigmentation of dominant transmission due to a disorder in melanocyte formation. Association of Prader-Willi syndrome with a chromosome abnormality in one of the subjects involved
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(P698) 413191
(P813) Friday, September 29, 2017

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(P698) 413191
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(P577) Thursday, December 1, 1977
(P248)
(P698) 413191
(P813) Friday, September 29, 2017

Saturday, December 31, 1977
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(P854) https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=413191
(P813) Wednesday, June 29, 2022

(P1476) "Familial oculo-cutaneous hypopigmentation of dominant transmission due to a disorder in melanocyte formation. Association of Prader-Willi syndrome with a chromosome abnormality in one of the subjects involved" (language: en)
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(P698) 413191
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(P813) Wednesday, June 29, 2022

(P2093) Frenk E
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Calame A
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(P698) 413191
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description scientific article published on December 31, 1977

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(P698) 413191