Concepedia

Contiguous gene syndrome due to an interstitial deletion in Xp22.3 in a boy with ichthyosis, chondrodysplasia punctata, mental retardation and ADHD

Fortunato Lonardo, Giancarlo Parenti, Daniela V. Luquetti, Ida Annunziata, Matteo Della Monica, Lucia Perone, Manuela De Gregori, Orsetta Zuffardi, Nicola Brunetti‐Pierri, Generoso Andria,

European Journal of Medical Genetics · 2007 · 41 citations · 13 references

DOI

Concepts

References

13

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

Stéphane Jamain, Hélène Quach, Catalina Betancur et al. · Nature Genetics · 2003 · 1.8K citations · Full text

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A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

Brunella Franco, Silvana Guioli, Antonella Pragliola et al. · Nature · 1991 · 851 citations

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X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family

Frédéric Laumonnier, Frédérique Bonnet‐Brilhault, Marie Gomot et al. · The American Journal of Human Genetics · 2004 · 760 citations · Full text

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A cluster of sulfatase genes on Xp22.3: Mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy

Brunella Franco, Germana Meroni, Giancarlo Parenti et al. · Cell · 1995 · 317 citations · Full text

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A Genomewide Scan for Loci Involved in Attention-Deficit/Hyperactivity Disorder

Simon E. Fisher, Clyde Francks, James T. McCracken et al. · The American Journal of Human Genetics · 2002 · 293 citations · Full text

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