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Clinical variability of Stickler syndrome with aCOL2A1 haploinsufficiency mutation: implications for genetic counselling
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http://hub.abes.fr/bmj/periodical/jmg/2000/volume_37/issue_4/w
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Title
Clinical variability of Stickler syndrome with aCOL2A1 haploinsufficiency mutation: implications for genetic counselling
has manifestation of work
http://hub.abes.fr/bmj/periodical/jmg/2000/volume_37/issue_4/B3598D6B5C407CBEE053120B220A90C5/m/web
http://hub.abes.fr/bmj/periodical/jmg/2000/volume_37/issue_4/B3598D6B5C407CBEE053120B220A90C5/m/print
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http://hub.abes.fr/bmj/periodical/jmg/2000/volume_37/issue_4/B3598D6B5C407CBEE053120B220A90C5/authorship/1
http://hub.abes.fr/bmj/periodical/jmg/2000/volume_37/issue_4/B3598D6B5C407CBEE053120B220A90C5/authorship/7
http://hub.abes.fr/bmj/periodical/jmg/2000/volume_37/issue_4/B3598D6B5C407CBEE053120B220A90C5/authorship/6
http://hub.abes.fr/bmj/periodical/jmg/2000/volume_37/issue_4/B3598D6B5C407CBEE053120B220A90C5/authorship/2
http://hub.abes.fr/bmj/periodical/jmg/2000/volume_37/issue_4/B3598D6B5C407CBEE053120B220A90C5/authorship/3
http://hub.abes.fr/bmj/periodical/jmg/2000/volume_37/issue_4/B3598D6B5C407CBEE053120B220A90C5/authorship/5
http://hub.abes.fr/bmj/periodical/jmg/2000/volume_37/issue_4/B3598D6B5C407CBEE053120B220A90C5/authorship/4
article type
letter
publisher identifier
9962
is part of this journal
Journal of Medical Genetics
PubMed ID
10819645
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