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4. Prenatal diagnosis of retinal detachment in Walker-Warburg syndrome. Farrell SA; Toi A; Leadman ML; Davidson RG; Caco C Am J Med Genet; 1987 Nov; 28(3):619-24. PubMed ID: 3122570 [TBL] [Abstract][Full Text] [Related]
5. Walker-Warburg syndrome (Warburg syndrome, HARD +/- E syndrome). Donnai D; Farndon PA J Med Genet; 1986 Jun; 23(3):200-3. PubMed ID: 3088278 [No Abstract] [Full Text] [Related]
6. 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]
7. Prenatal diagnosis of retinal nonattachment in the Walker-Warburg syndrome. Chitayat D; Toi A; Babul R; Levin A; Michaud J; Summers A; Rutka J; Blaser S; Becker LE Am J Med Genet; 1995 May; 56(4):351-8. PubMed ID: 7604843 [TBL] [Abstract][Full Text] [Related]
8. Clinical features of type 2 Stickler syndrome. Poulson AV; Hooymans JM; Richards AJ; Bearcroft P; Murthy R; Baguley DM; Scott JD; Snead MP J Med Genet; 2004 Aug; 41(8):e107. PubMed ID: 15286167 [No Abstract] [Full Text] [Related]
9. Hydrocephaly, congenital retinal nonattachment, and congenital falciform fold. Warburg M Am J Ophthalmol; 1978 Jan; 85(1):88-94. PubMed ID: 413438 [TBL] [Abstract][Full Text] [Related]
10. [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]
12. Absence of excess chromosome breakage in a patient with VACTERL-hydrocephalus. Evans JA; Chodirker BN Am J Med Genet; 1993 Aug; 47(1):112-3. PubMed ID: 8240537 [No Abstract] [Full Text] [Related]
13. [Atypical retinal detachment in an adolescent with thalidomide abnormalities]. Klaas D; Schütte E; Lizin F Ber Zusammenkunft Dtsch Ophthalmol Ges; 1977; 74():575-7. PubMed ID: 577782 [No Abstract] [Full Text] [Related]
14. VACTERL with hydrocephalus: one end of the Fanconi anemia spectrum of anomalies? Porteous ME; Cross I; Burn J Am J Med Genet; 1992 Aug; 43(6):1032-4. PubMed ID: 1415330 [TBL] [Abstract][Full Text] [Related]
15. [Prevention of retinal detachment in Wagner-Stickler syndrome]. Fritsch D; Vallat M; Lagoutte F; Verin P Bull Soc Ophtalmol Fr; 1989 May; 89(5):657-64. PubMed ID: 2590980 [No Abstract] [Full Text] [Related]
16. Hydrocephalus in an infant with trisomy 22. Fahmi F; Schmerler S; Hutcheon RG J Med Genet; 1994 Feb; 31(2):141-4. PubMed ID: 8182721 [TBL] [Abstract][Full Text] [Related]
17. Sagittal craniosynostosis, Dandy-Walker malformation, and hydrocephalus: a unique multiple malformation syndrome. Braddock SR; Jones KL; Superneau DW; Jones MC Am J Med Genet; 1993 Oct; 47(5):640-3; discussion 644. PubMed ID: 8266990 [TBL] [Abstract][Full Text] [Related]
18. Peculiar facial appearance, hydrocephalus, double-outlet right ventricle, genital anomalies and dense bones with lethal outcome. Beemer FA; von Ertbruggen I Am J Med Genet; 1984 Oct; 19(2):391-4. PubMed ID: 6507485 [No Abstract] [Full Text] [Related]
19. [Association of hereditary hydrocephalus and holoprosencephaly]. Lambert JC; Ferrari M; Donzeau M; Hericort P; Boutte P; Walbaum R; Ayraud N Arch Fr Pediatr; 1983 May; 40(5):397-9. PubMed ID: 6882130 [TBL] [Abstract][Full Text] [Related]
20. X-linked hydrocephalus and MASA syndrome present in one family are due to a single missense mutation in exon 28 of the L1CAM gene. Fransen E; Schrander-Stumpel C; Vits L; Coucke P; Van Camp G; Willems PJ Hum Mol Genet; 1994 Dec; 3(12):2255-6. PubMed ID: 7881431 [No Abstract] [Full Text] [Related] [Next] [New Search]