Wikidata

(Q34394203)

English

A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3.

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title
A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3. (English)
1 reference
stated in
Europe PubMed Central
PubMed ID
8776601
retrieved
1 August 2017

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