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2. Gillespie syndrome: a report of two further cases. Nelson J; Flaherty M; Grattan-Smith P Am J Med Genet; 1997 Aug; 71(2):134-8. PubMed ID: 9217210 [TBL] [Abstract][Full Text] [Related]
3. Syndrome of partial aniridia, cerebellar ataxia, and mental retardation--Gillespie syndrome. Nevin NC; Lim JH Am J Med Genet; 1990 Apr; 35(4):468-9. PubMed ID: 2333873 [TBL] [Abstract][Full Text] [Related]
5. Partial aniridia, cerebellar ataxia, and mental deficiency (Gillespie syndrome) in two brothers. Wittig EO; Moreira CA; Freire-Maia N; Vianna-Morgante AM Am J Med Genet; 1988 Jul; 30(3):703-8. PubMed ID: 3189393 [TBL] [Abstract][Full Text] [Related]
6. Megalocornea-mental retardation syndrome: an additional case. Antiñolo G; Rufo M; Borrego S; Morales C Am J Med Genet; 1994 Aug; 52(2):196-7. PubMed ID: 7802008 [TBL] [Abstract][Full Text] [Related]
7. [Gillespie syndrome (incomplete aniridia, cerebellar ataxia and oligophrenia)]. François J; Lentini F Klin Monbl Augenheilkd; 1984 Apr; 184(4):313-5. PubMed ID: 6727263 [TBL] [Abstract][Full Text] [Related]
8. [Genetic consequences of cosanguinity]. Maximilian C; Toncescu N; Pop TV; Duca-Marinescu D Rev Pediatr Obstet Ginecol Pediatr; 1976; 25(4):373-8. PubMed ID: 139666 [No Abstract] [Full Text] [Related]
9. Aplasia cutis congenita associated with limb, eye, and brain anomalies in sibs: a variant of the Adams-Oliver syndrome? Orstavik KH; Strömme P; Spetalen S; Flage T; Westvik J; Vesterhus P; Skjeldal O Am J Med Genet; 1995 Oct; 59(1):92-5. PubMed ID: 8849019 [TBL] [Abstract][Full Text] [Related]
10. Joubert syndrome: a major brain malformation. Ray J; Majumder AG; Das D; Mukhopadhyay D; Mondol S J Indian Med Assoc; 2007 Jul; 105(7):392-4. PubMed ID: 18178993 [TBL] [Abstract][Full Text] [Related]
14. Gillespie syndrome: An atypical form and review of the literature. Nabih O; Hamdani H; ELMaaloum L; Allali B; ELkettani A Ann Med Surg (Lond); 2022 Feb; 74():103244. PubMed ID: 35070290 [TBL] [Abstract][Full Text] [Related]
15. Lenz microphthalmia syndrome: three additional cases with rare associated anomalies. Temtamy SA; Ismail SI; Meguid NA Genet Couns; 2000; 11(2):147-52. PubMed ID: 10893665 [TBL] [Abstract][Full Text] [Related]
16. [Joubert syndrome: a report of 5 cases]. Calleja-Pérez B; Fernández-Jaén A; Martínez-Bermejo A; Pascual-Castroviejo I Rev Neurol; 1998 Apr; 26(152):548-50. PubMed ID: 9796002 [TBL] [Abstract][Full Text] [Related]
17. Thrombocytopenia-absent radius (tar) syndrome: a case with agenesis of corpus callosum, hypoplasia of cerebellar vermis and horseshoe kidney. Skórka A; Bielicka-Cymermann J; Gieruszczak-Białek D; Korniszewski L Genet Couns; 2005; 16(4):377-82. PubMed ID: 16440880 [TBL] [Abstract][Full Text] [Related]
18. COACH syndrome: report of two brothers with congenital hepatic fibrosis, cerebellar vermis hypoplasia, oligophrenia, ataxia, and mental retardation. Gentile M; Di Carlo A; Susca F; Gambotto A; Caruso ML; Panella C; Vajro P; Guanti G Am J Med Genet; 1996 Aug; 64(3):514-20. PubMed ID: 8862632 [TBL] [Abstract][Full Text] [Related]
19. [Cerebral and ocular abnormalities with anterior pituitary insufficiency of familial nature]. Weill J; Boudailliez B; Piussan C; Ponte C J Genet Hum; 1985 Jan; 33(1):31-5. PubMed ID: 3920352 [TBL] [Abstract][Full Text] [Related]
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