All individuals with variants in gene CCND2

2 entries on 1 page. Showing entries 1 - 2.
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AscendingIndividual ID     

ID_report     

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VIP     

Data_av     

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Owner     
00276047 - - - M - - - - - - - ? Lissencephaly (HP:0001339); Hydrocephalus (HP:0000238); Global developmental delay (HP:0001263); Astigmatism (HP:0000483) 1 1 IMGAG
00302976 Pat21 PubMed: Helbig 2016 - - - United States - - - - - seizures Epileptic encephalopathy, infantile spasms; age onset infantile 1 1 Johan den Dunnen
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