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http://hub.abes.fr/bmj/periodical/jmedgenet/1994/volume_31/issue_6/B35966E222B66AB5E053120B220AFD24/authorship/4
http://hub.abes.fr/bmj/periodical/archdischild/1983/volume_58/issue_12/B352B85B1BCD7B7FE053120B220AA14F/authorship/1
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http://hub.abes.fr/bmj/periodical/jmedgenet/1998/volume_35/issue_7/B3598D6B5A5C7CBEE053120B220A90C5/authorship/8
http://hub.abes.fr/bmj/periodical/gut/2001/volume_48/issue_1/B356B0251E783CE9E053120B220A6533/authorship/4
http://hub.abes.fr/bmj/periodical/jmg/2010/volume_47/issue_1/B3598D6B656D7CBEE053120B220A90C5/authorship/8
http://hub.abes.fr/bmj/periodical/gut/2013/volume_62/issue_6/B3571663E27E57DCE053120B220A2EA9/authorship/9
http://hub.abes.fr/bmj/periodical/jmedgenet/1993/volume_30/issue_10/B35966E2207A6AB5E053120B220AFD24/authorship/2
http://hub.abes.fr/bmj/periodical/heart/2010/volume_96/issue_20/B35772F80B7C2F84E053120B220A0936/authorship/12
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http://hub.abes.fr/bmj/periodical/bmj/2013/volume_346/issue_2013/B36F481D8B447DA4E053120B220A4C0F/authorship/1
http://hub.abes.fr/bmj/periodical/gut/2009/volume_58/issue_3/B356DBB034A2045AE053120B220A35DA/authorship/4
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http://hub.abes.fr/oup/periodical/brainj/2009/volume_132/issue_6/101093brainawn274/authorship/6
http://hub.abes.fr/oup/periodical/hmg/1997/volume_6/issue_1/101093hmg61105/authorship/6
http://hub.abes.fr/bmj/periodical/adc/1999/volume_81/issue_4/B35305B4333F0CF1E053120B220A6A4C/authorship/3
http://hub.abes.fr/bmj/periodical/gut/2008/volume_57/issue_5/B356DBB03332045AE053120B220A35DA/authorship/9
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http://hub.abes.fr/oup/periodical/carcin/1999/volume_20/issue_5/101093carcin205805/authorship/6
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http://hub.abes.fr/springer/periodical/10545/1994/volume_17/issue_4/B8DD76546FC22FF1E053120B220A8ECF/authorship/1
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of
Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutation
Isolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with DiGeorge syndrome
Life insurance and mortgage application in adults with congenital heart disease
European Code Against Cancer and scientific justification: third version (2003)
Intestinal tumorigenesis in the Apc1638N mouse treated with aspirin and resistant starch for up to 5 months
Four novel germ-line mutations in the APC gene detected by heteroduplex analysis
Genetic Mapping of the Human Homologue (T) of Mouse T(Brachyury) and a Search for Allele Association between Human T and Spina Bifida
Cancer Risk Associated with Germline DNA Mismatch Repair Gene Mutations
Relevance of the Human Genome Project to inherited metabolic disease
Interstitial deletions in DiGeorge syndrome detected with microclones from 22q11
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