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82. A linkage study of a large pedigree with X linked centronuclear myopathy. Starr J; Lamont M; Iselius L; Harvey J; Heckmatt J J Med Genet; 1990 May; 27(5):281-3. PubMed ID: 2352255 [TBL] [Abstract][Full Text] [Related]
83. [Clinical study of familial spastic paraplegia]. Mukai E; Takahashi A; Matsuo T Rinsho Shinkeigaku; 1987 Nov; 27(11):1399-406. PubMed ID: 3447800 [No Abstract] [Full Text] [Related]
85. Nephrogenic diabetes insipidus: close linkage with markers from the distal long arm of the human X chromosome. Knoers N; van der Heyden H; van Oost BA; Ropers HH; Monnens L; Willems J Hum Genet; 1988 Sep; 80(1):31-8. PubMed ID: 2843456 [TBL] [Abstract][Full Text] [Related]
86. Familial spastic paraplegia, bilateral sensorineural deafness, and intellectual retardation associated with a progressive nephropathy. Fitzsimmons JS; Watson AR; Mellor D; Guilbert PR J Med Genet; 1988 Mar; 25(3):168-72. PubMed ID: 3351903 [TBL] [Abstract][Full Text] [Related]
87. A novel mutation in exon 6 (F236S) of the proteolipid protein gene is associated with spastic paraplegia. Donnelly A; Colley A; Crimmins D; Mulley J Hum Mutat; 1996; 8(4):384-5. PubMed ID: 8956049 [No Abstract] [Full Text] [Related]
89. X-linked mental retardation with dystonic movements of the hands. Partington MW; Mulley JC; Sutherland GR; Hockey A; Thode A; Turner G Am J Med Genet; 1988; 30(1-2):251-62. PubMed ID: 3177452 [TBL] [Abstract][Full Text] [Related]
90. [Familial spastic paraplegia. A case report]. Luo DR; Hu CH Hua Xi Yi Ke Da Xue Xue Bao; 1987 Mar; 18(1):93-5. PubMed ID: 3623530 [No Abstract] [Full Text] [Related]
91. X linked neonatal centronuclear/myotubular myopathy: evidence for linkage to Xq28 DNA marker loci. Thomas NS; Williams H; Cole G; Roberts K; Clarke A; Liechti-Gallati S; Braga S; Gerber A; Meier C; Moser H J Med Genet; 1990 May; 27(5):284-7. PubMed ID: 2352256 [TBL] [Abstract][Full Text] [Related]
92. Spastic paraplegia, glaucoma and mental retardation--in three siblings. A new genetic syndrome. Heijbel J; Jagell S Hereditas; 1981; 94(2):203-7. PubMed ID: 7298353 [No Abstract] [Full Text] [Related]
93. Towards fully automated genotyping: use of an X linked recessive spastic paraplegia family to test alternative analysis methods. Kobayashi H; Matise TC; Perlin MW; Marks HG; Hoffman EP Hum Genet; 1995 May; 95(5):483-90. PubMed ID: 7759066 [TBL] [Abstract][Full Text] [Related]
95. Heterogeneity of X-linked recessive (spino)cerebellar ataxia with or without spastic diplegia. Apak S; Yüksel M; Ozmen M; Saka N; Darendeliler F; Neuhäuser G Am J Med Genet; 1989 Oct; 34(2):155-8. PubMed ID: 2816991 [TBL] [Abstract][Full Text] [Related]
96. Allan-Herndon-Dudley syndrome: clinical and linkage studies on a second family. Bialer MG; Lawrence L; Stevenson RE; Silverberg G; Williams MK; Arena JF; Lubs HA; Schwartz CE Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):491-7. PubMed ID: 1605231 [TBL] [Abstract][Full Text] [Related]
97. Reevaluation of a large family defines a new locus for X-linked recessive pure spastic paraplegia (SPG34) on chromosome Xq25. Macedo-Souza LI; Kok F; Santos S; Licinio L; Lezirovitz K; Nascimento RM; Bueno C; Martyn M; Leão EK; Zatz M Neurogenetics; 2008 Jul; 9(3):225-6. PubMed ID: 18463901 [No Abstract] [Full Text] [Related]
98. Heredofamilial syndrome of spastic paraplegia, dysarthria and cutaneous lesions in ive siblings. Bahemuka M; Brown JD Dev Med Child Neurol; 1982 Aug; 24(4):519-24. PubMed ID: 7117711 [TBL] [Abstract][Full Text] [Related]
99. Familial spastic paraplegia with amyotrophy of the hands. Silver JR Ann Hum Genet; 1966 Jul; 30(1):69-75. PubMed ID: 5964029 [No Abstract] [Full Text] [Related]
100. X-linked spastic paraplegia due to a mutation (C506T; Ser169Phe) in exon 4 of the proteolipid protein gene (PLP). Hodes ME; Hadjisavvas A; Butler IJ; Aydanian A; Dlouhy SR Am J Med Genet; 1998 Feb; 75(5):516-7. PubMed ID: 9489796 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]