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3. [Holoprosencephaly, polydactyly, cardiopathy: new syndrome or a new case of hydrolethalus?]. André SA; Cordier MP; Beaufrère AM; Guillaud M; Robert JM J Genet Hum; 1988 Dec; 36(5):463-8. PubMed ID: 3216192 [TBL] [Abstract][Full Text] [Related]
5. Congenital hydrocephalus and eye abnormalities with severe developmental brain defects: Warburg's syndrome. Bordarier C; Aicardi J; Goutieres F Ann Neurol; 1984 Jul; 16(1):60-5. PubMed ID: 6431899 [TBL] [Abstract][Full Text] [Related]
6. [The hydrolethalus syndrome--a new hereditary malformation syndrome in Finland]. Salonen R; Herva R; Norio R Duodecim; 1981; 97(16):1312-9. PubMed ID: 7327122 [No Abstract] [Full Text] [Related]
7. Hydrolethalus syndrome: report of an apparent mild case, literature review, and differential diagnosis. Aughton DJ; Cassidy SB Am J Med Genet; 1987 Aug; 27(4):935-42. PubMed ID: 3321994 [TBL] [Abstract][Full Text] [Related]
8. Brief clinical report: HARD (+/- E) syndrome: report of a sixth family with support for autosomal-recessive inheritance. Aymé S; Mattei JF Am J Med Genet; 1983 Apr; 14(4):759-66. PubMed ID: 6405616 [TBL] [Abstract][Full Text] [Related]
9. Holoprosencephaly and polydactyly: a possible expression of the hydrolethalus syndrome. Bachman H; Clark RD; Salahi W J Med Genet; 1990 Jan; 27(1):50-2. PubMed ID: 2407847 [TBL] [Abstract][Full Text] [Related]
10. Joubert syndrome: more than lower cerebellar vermis hypoplasia, less than a complex brain malformation. Boltshauser E Am J Med Genet; 2002 May; 109(4):332. PubMed ID: 11992490 [No Abstract] [Full Text] [Related]
12. Shprintzen-Goldberg syndrome with osteopenia and progressive hydrocephalus. Hassed S; Shewmake K; Teo C; Curtis M; Cunniff C Am J Med Genet; 1997 Jun; 70(4):450-3. PubMed ID: 9182791 [No Abstract] [Full Text] [Related]
13. Follow-up of an adult with Keutel syndrome. Devriendt K; Holvoet M; Fryns JP Am J Med Genet; 1999 Jul; 85(1):82-3. PubMed ID: 10377017 [No Abstract] [Full Text] [Related]
16. Hydrolethalus syndrome: neuropathology of 21 cases confirmed by HYLS1 gene mutation analysis. Paetau A; Honkala H; Salonen R; Ignatius J; Kestilä M; Herva R J Neuropathol Exp Neurol; 2008 Aug; 67(8):750-62. PubMed ID: 18648327 [TBL] [Abstract][Full Text] [Related]
17. Siblings with a syndrome of hydrocephalus with patent aqueduct, growth retardation and associated anomalies. Slee J; Knowles S; Goldblatt J Clin Dysmorphol; 1999 Jan; 8(1):11-4. PubMed ID: 10327245 [TBL] [Abstract][Full Text] [Related]
18. Bilateral pulmonary agenesis: association with the hydrolethalus syndrome and review of the literature from a developmental field perspective. Toriello HV; Bauserman SC Am J Med Genet; 1985 May; 21(1):93-103. PubMed ID: 4003452 [TBL] [Abstract][Full Text] [Related]