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2. [X-linked hydrocephalus (Brickers-Adams syndrome). A case report confirmed by molecular genetic studies]. Santos F; Temudo T Rev Neurol; 2000 Dec 1-15; 31(11):1039-42. PubMed ID: 11190871 [TBL] [Abstract][Full Text] [Related]
3. The spectrum of "complicated spastic paraplegia, MASA syndrome and X-linked hydrocephalus". Contribution of DNA linkage analysis in genetic counseling of individual families. Schrander-Stumpel C; Meyer H; Merckx D; Jones M; Israel J; Sommer A; Stevens C; Tinschert S; Wilson G; Willems P Genet Couns; 1994; 5(1):1-10. PubMed ID: 8031529 [TBL] [Abstract][Full Text] [Related]
8. Genetic heterogeneity in X-linked hydrocephalus: linkage to markers within Xq27.3. Strain L; Gosden CM; Brock DJ; Bonthron DT Am J Hum Genet; 1994 Feb; 54(2):236-43. PubMed ID: 8304340 [TBL] [Abstract][Full Text] [Related]
9. Hydrocephalus, skeletal anomalies, and mental disturbances in a mother and three daughters: a new syndrome. Ferlini A; Ragno M; Gobbi P; Marinucci C; Rossi R; Zanetti A; Milan M; Camera G; Calzolari E Am J Med Genet; 1995 Dec; 59(4):506-11. PubMed ID: 8585573 [TBL] [Abstract][Full Text] [Related]
10. Fried syndrome is a distinct X linked mental retardation syndrome mapping to Xp22. Strain L; Wright AF; Bonthron DT J Med Genet; 1997 Jul; 34(7):535-40. PubMed ID: 9222959 [TBL] [Abstract][Full Text] [Related]
11. X-linked hydrocephalus: clinical heterogeneity at a single gene locus. Serville F; Lyonnet S; Pelet A; Reynaud M; Louail C; Munnich A; Le Merrer M Eur J Pediatr; 1992 Jul; 151(7):515-8. PubMed ID: 1396913 [TBL] [Abstract][Full Text] [Related]
12. Corpus callosum agenesis, spastic quadriparesis and irregular lining of the lateral ventricles on CT-scan. A distinct X-linked mental retardation syndrome? Vles JS; Fryns JP; Folmer K; Boon P; Buttiens M; Grubben C; Janevski B Genet Couns; 1990; 1(2):97-102. PubMed ID: 2081003 [TBL] [Abstract][Full Text] [Related]
13. X-linked hydrocephalus, with aqueductal stenosis, mental retardation, and adduction-flexion deformity of the thumbs. Report of a family. Faivre J; Lemarec B; Bretagne J; Pecker J Childs Brain; 1976; 2(4):226-33. PubMed ID: 991665 [TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis of X linked hydrocephalus without aqueductal stenosis. Váradi V; Csécsei K; Szeifert GT; Tóth Z; Papp Z J Med Genet; 1987 Apr; 24(4):207-9. PubMed ID: 3295245 [TBL] [Abstract][Full Text] [Related]
16. Ciliary dyskinesia associated with hydrocephalus and mental retardation in a Jordanian family. al-Shroof M; Karnik AM; Karnik AA; Longshore J; Sliman NA; Khan FA Mayo Clin Proc; 2001 Dec; 76(12):1219-24. PubMed ID: 11761503 [TBL] [Abstract][Full Text] [Related]
17. A new X-linked mental retardation syndrome. Homfray T; Holland T; Patton M Clin Dysmorphol; 1995 Oct; 4(4):289-93. PubMed ID: 8574418 [TBL] [Abstract][Full Text] [Related]
18. X-linked recessive inheritance of dysgenesis of corpus callosum in a Chinese family. Kang WM; Huang CC; Lin SJ Am J Med Genet; 1992 Nov; 44(5):619-23. PubMed ID: 1481821 [TBL] [Abstract][Full Text] [Related]
19. Possible linkage between Xg and the locus for a gene causing mental retardation with or without hydrocephalus. Fried K; Sanger R J Med Genet; 1973 Mar; 10(1):17-8. PubMed ID: 4697849 [TBL] [Abstract][Full Text] [Related]
20. Spondylo-epimetaphyseal dysplasia: a new X-linked variant with mental retardation. Bieganski T; Dawydzik B; Kozlowski K Eur J Pediatr; 1999 Oct; 158(10):809-14. PubMed ID: 10486082 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]