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http://hub.abes.fr/bmj/periodical/jmedgenet/1995/volume_32/issue_10/B35966E223426AB5E053120B220AFD24/authorship/4
http://hub.abes.fr/bmj/periodical/jmedgenet/1997/volume_34/issue_6/B35966E226876AB5E053120B220AFD24/authorship/1
http://hub.abes.fr/oup/periodical/hmg/2000/volume_9/issue_2/101093hmg92165/authorship/4
http://hub.abes.fr/oup/periodical/cercor/2008/volume_18/issue_7/101093cercorbhm184/authorship/6
http://hub.abes.fr/oup/periodical/hmg/1992/volume_1/issue_9/101093hmg19776/authorship/5
http://hub.abes.fr/bmj/periodical/jmg/2000/volume_37/issue_8/B3598D6B5C887CBEE053120B220A90C5/authorship/5
http://hub.abes.fr/oup/periodical/hmg/1998/volume_7/issue_5/101093hmg75813/authorship/2
http://hub.abes.fr/oup/periodical/hmg/2002/volume_11/issue_22/101093hmg11222793/authorship/11
http://hub.abes.fr/oup/periodical/hmg/2010/volume_19/issue_2/101093hmgddp500/authorship/4
http://hub.abes.fr/oup/periodical/hmg/1992/volume_1/issue_9/101093hmg19778/authorship/5
http://hub.abes.fr/oup/periodical/hmg/1993/volume_2/issue_1/101093hmg2192a/authorship/5
http://hub.abes.fr/oup/periodical/hmg/1993/volume_2/issue_5/101093hmg25613/authorship/6
http://hub.abes.fr/oup/periodical/hmg/2000/volume_9/issue_5/101093hmg95695/authorship/11
http://hub.abes.fr/bmj/periodical/jmedgenet/1993/volume_30/issue_12/B35966E220B86AB5E053120B220AFD24/authorship/6
http://hub.abes.fr/springer/periodical/439/1993/volume_90/issue_5/B9279D37F7D85861E053120B220A3025/authorship/3
http://hub.abes.fr/springer/periodical/439/1992/volume_88/issue_3/B927678D91695706E053120B220AC130/authorship/1
http://hub.abes.fr/springer/periodical/439/1989/volume_81/issue_3/B9279D37F73E5861E053120B220A3025/authorship/1
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A Novel Mammalian Wnt Gene, WNT8B, Shows Brain-Restricted Expression in Early Development, with Sharply Delimited Expression Boundaries in the Developing Forebrain
Human-mouse differences in the embryonic expression patterns of developmental control genes and disease genes
Dinucleotide repeat polymorphism at the DXS556 locus
Craniofacial expression of human and murine TBX22 correlates with the cleft palate and ankyloglossia phenotype observed in CPX patients
The nystagmus-associated FRMD7 gene regulates neuronal outgrowth and development
Two dinucleotide repeat polymorphisms at the DXS571 locus
The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome
A Molecular Neuroanatomical Study of the Developing Human Neocortex from 8 to 17 Postconceptional Weeks Revealing the Early Differentiation of the Subplate and Subventricular Zone
Dinucleotide repeat polymorphism at the DXS559 locus
Dinucleotide repeat polymorphism at the DXS573 locus
Localisation of the gene for Norrie disease to between DXS7 and DXS426 on Xp
Til 1 — a human lymphoblastoid cell line with minimal DNA methylation
X chromosome linkage studies in familial Rett syndrome
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