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Items: 3

1.

#616004 - DYSFIBRINOGENEMIA, CONGENITAL

HYPODYSFIBRINOGENEMIA, CONGENITAL, INCLUDED

Cytogenetic locations: STQTL12, STQTL12, 1p36

2.

#202400 - AFIBRINOGENEMIA, CONGENITAL

HYPOFIBRINOGENEMIA, CONGENITAL, INCLUDED

Cytogenetic locations: at, lod, max

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