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46. MASA syndrome: new clinical features and linkage analysis using DNA probes. Schrander-Stumpel C; Legius E; Fryns JP; Cassiman JJ J Med Genet; 1990 Nov; 27(11):688-92. PubMed ID: 2277384 [TBL] [Abstract][Full Text] [Related]
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54. Linkage and genetic counselling for the fragile X using DNA probes 52A, F9, DX13, and ST14. Mulley JC; Gedeon AK; Thorn KA; Bates LJ; Sutherland GR Am J Med Genet; 1987 Jun; 27(2):435-48. PubMed ID: 2886048 [TBL] [Abstract][Full Text] [Related]
55. Family with Pelizaeus-Merzbacher disease/X-linked spastic paraplegia and a nonsense mutation in exon 6 of the proteolipid protein gene. Bond C; Si X; Crisp M; Wong P; Paulson GW; Boesel CP; Dlouhy SR; Hodes ME Am J Med Genet; 1997 Aug; 71(3):357-60. PubMed ID: 9268109 [TBL] [Abstract][Full Text] [Related]
56. Familial spastic paraplegia on Mitiaro, Cook Islands. Kuberski T; Tetava P; Koteka G N Z Med J; 1981 Mar; 93(680):187-8. PubMed ID: 6941104 [TBL] [Abstract][Full Text] [Related]
57. Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers. Hentati A; Pericak-Vance MA; Lennon F; Wasserman B; Hentati F; Juneja T; Angrist MH; Hung WY; Boustany RM; Bohlega S Hum Mol Genet; 1994 Oct; 3(10):1867-71. PubMed ID: 7849714 [TBL] [Abstract][Full Text] [Related]
58. Four brothers with mental retardation, spastic paraplegia and palmoplantar hyperkeratosis. A new syndrome? Fitzsimmons JS; Fitzsimmons EM; McLachlan JI; Gilbert GB Clin Genet; 1983 Apr; 23(4):329-35. PubMed ID: 6221837 [TBL] [Abstract][Full Text] [Related]
59. Linkage analysis using multiple Xq DNA polymorphisms in normal families, families with the fragile X syndrome, and other families with X linked conditions. Connor JM; Pirrit LA; Yates JR; Crossley JA; Imrie SJ; Colgan JM J Med Genet; 1987 Jan; 24(1):14-22. PubMed ID: 2879932 [TBL] [Abstract][Full Text] [Related]
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