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M Muenke

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Molecular Psychiatry|May 25, 2011

A cooperative interaction between LPHN3 and 11q doubles the risk for ADHDM Jain, J I Vélez, M T Acosta, et al.

American Journal of Human Genetics|March 1, 1997

A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndromeM Muenke, K W Gripp, D M McDonald-McGinn, et al.

Molecular Psychiatry|February 17, 2010

A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medicationM Arcos-Burgos, M Jain, M T Acosta, et al.

Journal of Medical Genetics|April 7, 2009

Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and functionF Lacbawan, B D Solomon, E Roessler, et al.

Pageof 11

Search research articles

Showing results (101-110 of 104) with videos related to

Sort By:

Pageof 11

You have reached the last page of results.This site can display upto 104 results.

Molecular Psychiatry|May 25, 2011

A cooperative interaction between LPHN3 and 11q doubles the risk for ADHDM Jain, J I Vélez, M T Acosta, et al.

American Journal of Human Genetics|March 1, 1997

A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndromeM Muenke, K W Gripp, D M McDonald-McGinn, et al.

Molecular Psychiatry|February 17, 2010

A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medicationM Arcos-Burgos, M Jain, M T Acosta, et al.

Journal of Medical Genetics|April 7, 2009

Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and functionF Lacbawan, B D Solomon, E Roessler, et al.

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