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CLINICAL GENETICS, ISSN 0009-9163, 11/2018, Volume 94, Issue 5, pp. 450 - 456
MED12 is a member of the large Mediator complex that controls cell growth, development, and differentiation. Mutations in MED12 disrupt neuronal gene... 
MED12 | molecular modeling | Lujan-Fryns syndrome | Ohdo syndrome | MUTATION | GENETICS & HEREDITY | FG syndrome | X-linked intellectual disability
Journal Article
Nature genetics, ISSN 1061-4036, 2014, Volume 46, Issue 8, pp. 815 - 817
Journal Article
Clinical Genetics, ISSN 0009-9163, 11/2018, Volume 94, Issue 5, pp. 450 - 456
MED12 is a member of the large Mediator complex that controls cell growth, development, and differentiation. Mutations in MED12 disrupt neuronal gene... 
MED12 | FG syndrome | Lujan‐Fryns syndrome | molecular modeling | Ohdo syndrome | X‐linked intellectual disability | X-linked intellectual disability | Lujan-Fryns syndrome | Medicine, Experimental | Medical research | Gene expression | Analysis | Prognathism | Molecular modelling | Blood cells
Journal Article
Journal Article
Nature Genetics, ISSN 1061-4036, 09/2007, Volume 39, Issue 9, pp. 1127 - 1133
Journal Article
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, ISSN 1552-4825, 12/2013, Volume 161, Issue 12, pp. 3063 - 3071
FG syndrome, Lujan syndrome, and Ohdo syndrome, the Maat-Kievit-Brunner type, have been described as distinct syndromes with overlapping non-specific features... 
MED12 | YWHAE | 17p13 | DELINEATION | MENTAL-RETARDATION | GENETICS & HEREDITY | X-linked | intellectual deficiency | EXPRESSION | FG SYNDROME | Cognitive science
Journal Article
Journal Article