A novel homozygous HOXB1 mutation in a Turkish family with hereditary congenital facial paresis.
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A novel homozygous HOXB1 mutation in a Turkish family with hereditary congenital facial paresis.
description
2016 nî lūn-bûn
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2016年の論文
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2016年学术文章
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2016年学术文章
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2016年学术文章
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2016年学术文章
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2016年学术文章
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2016年学术文章
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2016年學術文章
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2016年學術文章
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name
A novel homozygous HOXB1 mutat ...... ary congenital facial paresis.
@en
A novel homozygous HOXB1 mutat ...... ary congenital facial paresis.
@nl
type
label
A novel homozygous HOXB1 mutat ...... ary congenital facial paresis.
@en
A novel homozygous HOXB1 mutat ...... ary congenital facial paresis.
@nl
prefLabel
A novel homozygous HOXB1 mutat ...... ary congenital facial paresis.
@en
A novel homozygous HOXB1 mutat ...... ary congenital facial paresis.
@nl
P2093
P1476
A novel homozygous HOXB1 mutat ...... ary congenital facial paresis.
@en
P2093
Bedia Sahin
Gülay Güngör
Olcay Güngör
Serdar Ceylaner
Yavuz Sahin
P304
P356
10.1016/J.BRAINDEV.2016.09.002
P577
2016-09-15T00:00:00Z