Similar articles

• Hypergonadotropic hypogonadism in oligophrenia.

  Lundberg PO, Nilsson AC, Wide L. Lundberg PO, et al. Acta Med Scand. 1978;204(1-2):115-21. doi: 10.1111/j.0954-6820.1978.tb08409.x. Acta Med Scand. 1978. PMID: 685719
• New autosomal recessive syndrome of mental retardation, epilepsy, short stature, and skeletal dysplasia.

  Gurrieri F, Sammito V, Bellussi A, Neri G. Gurrieri F, et al. Am J Med Genet. 1992 Oct 1;44(3):315-20. doi: 10.1002/ajmg.1320440310. Am J Med Genet. 1992. PMID: 1488978 No abstract available.
• Syndrome of pigmentary retinal degeneration, cataract, microcephaly, and severe mental retardation.

  Mirhosseini SA, Holmes LB, Walton DS. Mirhosseini SA, et al. J Med Genet. 1972 Jun;9(2):193-6. doi: 10.1136/jmg.9.2.193. J Med Genet. 1972. PMID: 5046629 Free PMC article. No abstract available.
• Genetic disorders associated with postnatal microcephaly.

  Seltzer LE, Paciorkowski AR. Seltzer LE, et al. Am J Med Genet C Semin Med Genet. 2014 Jun;166C(2):140-55. doi: 10.1002/ajmg.c.31400. Epub 2014 May 16. Am J Med Genet C Semin Med Genet. 2014. PMID: 24839169 Review.
• RAB3GAP1, RAB3GAP2 and RAB18: disease genes in Micro and Martsolf syndromes.

  Handley MT, Aligianis IA. Handley MT, et al. Biochem Soc Trans. 2012 Dec 1;40(6):1394-7. doi: 10.1042/BST20120169. Biochem Soc Trans. 2012. PMID: 23176487 Review.