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2. Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1. Farooq M; Baig S; Tommerup N; Kjaer KW Am J Med Genet A; 2010 Feb; 152A(2):495-7. PubMed ID: 20101680 [No Abstract] [Full Text] [Related]
4. Combined deletion of two Condensin II system genes (NCAPG2 and MCPH1) in a case of severe microcephaly and mental deficiency. Perche O; Menuet A; Marcos M; Liu L; Pâris A; Utami KH; Kervran D; Cacheux V; Laudier B; Briault S Eur J Med Genet; 2013 Nov; 56(11):635-41. PubMed ID: 24013099 [TBL] [Abstract][Full Text] [Related]
5. Microcephaly genes and the evolution of sexual dimorphism in primate brain size. Montgomery SH; Mundy NI J Evol Biol; 2013 Apr; 26(4):906-11. PubMed ID: 23305468 [TBL] [Abstract][Full Text] [Related]
8. A common mechanism for microcephaly. Wollnik B Nat Genet; 2010 Nov; 42(11):923-4. PubMed ID: 20980985 [No Abstract] [Full Text] [Related]
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10. Evolution. Are human brains still evolving? Brain genes show signs of selection. Balter M Science; 2005 Sep; 309(5741):1662-3. PubMed ID: 16150985 [No Abstract] [Full Text] [Related]
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16. ASPM mutations identified in patients with primary microcephaly and seizures. Shen J; Eyaid W; Mochida GH; Al-Moayyad F; Bodell A; Woods CG; Walsh CA J Med Genet; 2005 Sep; 42(9):725-9. PubMed ID: 16141009 [TBL] [Abstract][Full Text] [Related]
17. Primary microcephaly with anterior predominant pachygyria caused by novel compound heterozygous mutations in ASPM. Nakamura K; Inui T; Miya F; Kanemura Y; Okamoto N; Saitoh S; Yamasaki M; Tsunoda T; Kosaki K; Tanaka S; Kato M Pediatr Neurol; 2015 May; 52(5):e7-8. PubMed ID: 25765464 [No Abstract] [Full Text] [Related]
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