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Q37718486-2FFC5172-1FDC-402D-8B74-9F1D8F999317
Q37718486-2FFC5172-1FDC-402D-8B74-9F1D8F999317
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Statement
http://www.wikidata.org/entity/statement/Q37718486-2FFC5172-1FDC-402D-8B74-9F1D8F999317
Whole exome sequencing in a patient with uniparental disomy of chromosome 2 and a complex phenotype.
P2860
Q37718486-2FFC5172-1FDC-402D-8B74-9F1D8F999317
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37718486-2FFC5172-1FDC-402D-8B74-9F1D8F999317
rank
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type
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Statement
wasDerivedFrom
ac71e4d34ef6d43b97341f0ee0ab9f2827d60e57
P2860
Maternal isodisomy for chromosome 2p causing severe congenital hypothyroidism.