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3. New neurological findings in trisomy 13. Gilbert LA; Dudley AW; Meisner L; Viseskul C; de Venecia G Arch Pathol Lab Med; 1977 Oct; 101(10):540-4. PubMed ID: 578686 [TBL] [Abstract][Full Text] [Related]
4. Central nervous system abnormalities in trisomy E (17-18) syndrome. Michaelson PS; Gilles FH J Neurol Sci; 1972 Feb; 15(2):193-208. PubMed ID: 5010105 [No Abstract] [Full Text] [Related]
5. Long survival with cerebellar aplasia and degenerative changes of CNS. A case report. Adamek D; Zulichowski S; Kałuza J Neuropatol Pol; 1986; 24(1):89-100. PubMed ID: 3748407 [No Abstract] [Full Text] [Related]
6. [Present-day neurological anatomy of schizophrenia (review of foreign literature]. Orlovskaia DD; Uranova NA Zh Nevropatol Psikhiatr Im S S Korsakova; 1990; 90(10):114-20. PubMed ID: 1962987 [No Abstract] [Full Text] [Related]
7. Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations. Hong SE; Shugart YY; Huang DT; Shahwan SA; Grant PE; Hourihane JO; Martin ND; Walsh CA Nat Genet; 2000 Sep; 26(1):93-6. PubMed ID: 10973257 [TBL] [Abstract][Full Text] [Related]
8. Mediobasal prosencephalic defects, including holoprosencephaly and cyclopia, in relation to the development of the human forebrain. Müller F; O'Rahilly R Am J Anat; 1989 Aug; 185(4):391-414. PubMed ID: 2506752 [TBL] [Abstract][Full Text] [Related]
9. Cerebello-cortical heterotopia in dentate nucleus, and other microdysgeneses in trisomy D1 (Patau) syndrome. Hori A; Peiffer J; Pfeiffer RA; Iizuka R Brain Dev; 1980; 2(4):345-52. PubMed ID: 7224090 [TBL] [Abstract][Full Text] [Related]
11. Genetic counselling in holoprosencephaly. Burck U Helv Paediatr Acta; 1982 Jun; 37(3):231-7. PubMed ID: 7118555 [TBL] [Abstract][Full Text] [Related]
12. [Neurenteric cyst of the medulla oblongata as an element of multiple developmental brain defects]. Zalatnai A Morphol Igazsagugyi Orv Sz; 1984 Apr; 24(2):111-8. PubMed ID: 6717446 [No Abstract] [Full Text] [Related]