Novel mutation in ABBC9 gene associated with congenital hypertrichosis and acromegaloid facial features, without cardiac or skeletal anomalies: a new phenotype.
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Novel mutation in ABBC9 gene associated with congenital hypertrichosis and acromegaloid facial features, without cardiac or skeletal anomalies: a new phenotype.
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2018 nî lūn-bûn
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name
Novel mutation in ABBC9 gene a ...... al anomalies: a new phenotype.
@en
Novel mutation in ABBC9 gene a ...... al anomalies: a new phenotype.
@nl
type
label
Novel mutation in ABBC9 gene a ...... al anomalies: a new phenotype.
@en
Novel mutation in ABBC9 gene a ...... al anomalies: a new phenotype.
@nl
prefLabel
Novel mutation in ABBC9 gene a ...... al anomalies: a new phenotype.
@en
Novel mutation in ABBC9 gene a ...... al anomalies: a new phenotype.
@nl
P2860
P50
P356
P1476
Novel mutation in ABBC9 gene a ...... tal anomalies: a new phenotype
@en
P2093
Claudia L Montoya
Harry Pachajoa
P2860
P356
10.2147/TACG.S155022
P577
2018-03-23T00:00:00Z