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European Journal of Medical Genetics|April 14, 2009
Fragile X syndrome screening of families with consanguineous and non-consanguineous parents in the Iranian populationAli Reza Pouya, Seyedeh Sedigheh Abedini, Neda Mansoorian, et al.
American Journal of Human Genetics|November 25, 2003
Mutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardationSarah A Shoichet, Kirsten Hoffmann, Corinna Menzel, et al.
American Journal of Human Genetics|May 27, 2004
Mutations in the FTSJ1 gene coding for a novel S-adenosylmethionine-binding protein cause nonsyndromic X-linked mental retardationKristine Freude, Kirsten Hoffmann, Lars-Riff Jensen, et al.
Human Mutation|July 11, 2008
A balanced chromosomal translocation disrupting ARHGEF9 is associated with epilepsy, anxiety, aggression, and mental retardationVera M Kalscheuer, Luciana Musante, Cheng Fang, et al.
European Journal of Medical Genetics|November 6, 2007
Screening of 20 patients with X-linked mental retardation using chromosome X-specific array-MAPHLudmila Kousoulidou, Sven Parkel, Olga Zilina, et al.
The Journal of Clinical Investigation|April 9, 2013
CCDC22 deficiency in humans blunts activation of proinflammatory NF-κB signalingPetro Starokadomskyy, Nathan Gluck, Haiying Li, et al.
American Journal of Human Genetics|September 12, 2007
A defect in the ionotropic glutamate receptor 6 gene (GRIK2) is associated with autosomal recessive mental retardationMohammad Mahdi Motazacker, Benjamin Rainer Rost, Tim Hucho, et al.
Zeitschrift Fur Kinder- Und Jugendpsychiatrie Und Psychotherapie|November 11, 2020
A Novel Locus and Candidate Gene for Familial Developmental Dyslexia on Chromosome 4qTiemo Grimm, Masoud Garshasbi, Lucia Puettmann, et al.
Human Molecular Genetics|July 3, 2014
Epigenetic remodelling and dysregulation of DLGAP4 is linked with early-onset cerebellar ataxiaSheroy Minocherhomji, Claus Hansen, Hyung-Goo Kim, et al.
American Journal of Human Genetics|January 20, 2007
Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndromeEva Klopocki, Harald Schulze, Gabriele Strauss, et al.
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