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Q35906602-0A42D32D-9F33-4262-96E3-2916D045BB0A
Q35906602-0A42D32D-9F33-4262-96E3-2916D045BB0A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35906602-0A42D32D-9F33-4262-96E3-2916D045BB0A
A recurrent deletion on chromosome 2q13 is associated with developmental delay and mild facial dysmorphisms.
P2860
Q35906602-0A42D32D-9F33-4262-96E3-2916D045BB0A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35906602-0A42D32D-9F33-4262-96E3-2916D045BB0A
rank
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Statement
wasDerivedFrom
1776014ac7fcb302e924ddecdb493a36847928fc
P2860
Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformations.