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ASALL1 mutation causes a branchio-oto-renal syndrome-like phenotype
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http://hub.abes.fr/bmj/periodical/jmg/2000/volume_37/issue_6/w
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Title
ASALL1 mutation causes a branchio-oto-renal syndrome-like phenotype
has manifestation of work
http://hub.abes.fr/bmj/periodical/jmg/2000/volume_37/issue_6/B3598D6B5C667CBEE053120B220A90C5/m/print
http://hub.abes.fr/bmj/periodical/jmg/2000/volume_37/issue_6/B3598D6B5C667CBEE053120B220A90C5/m/web
related by
http://hub.abes.fr/bmj/periodical/jmg/2000/volume_37/issue_6/B3598D6B5C667CBEE053120B220A90C5/authorship/1
http://hub.abes.fr/bmj/periodical/jmg/2000/volume_37/issue_6/B3598D6B5C667CBEE053120B220A90C5/authorship/2
http://hub.abes.fr/bmj/periodical/jmg/2000/volume_37/issue_6/B3598D6B5C667CBEE053120B220A90C5/authorship/3
article type
letter
publisher identifier
0043
is part of this journal
Journal of Medical Genetics
PubMed ID
10928856
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