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31. Identification of 7th hexosaminidase A mutation of Tay-Sachs disease in the Turkish population. Sinici I; Onder E; Topçu M; Ozkara HA Turk J Pediatr; 2007; 49(3):337-8. PubMed ID: 17990595 [No Abstract] [Full Text] [Related]
33. [Niemann-Pick and Tay-Sachs syndromes; intermediary forms and etiopathogenetic relations between the two syndromes in a case recently studied]. SALOMONE P Minerva Pediatr; 1954 Feb; 6(3):90-5. PubMed ID: 13154134 [No Abstract] [Full Text] [Related]
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37. Allogeneic BMT followed by substrate reduction therapy in a child with subacute Tay-Sachs disease. Jacobs JF; Willemsen MA; Groot-Loonen JJ; Wevers RA; Hoogerbrugge PM Bone Marrow Transplant; 2005 Nov; 36(10):925-6. PubMed ID: 16151419 [No Abstract] [Full Text] [Related]
38. Detection of trisomy 21 in a fetus during the investigation for Tay-Sachs disease. Alpman A; Bora E; Karaca E; Cankaya T; Onay H; Cogulu O; Gunduz C; Kleijer WJ; Ozkinay F Genet Couns; 2004; 15(1):99-100. PubMed ID: 15083708 [No Abstract] [Full Text] [Related]
39. Tay-Sachs' Disease: A Study of the Symptomatology and Pathology of Three Atypical Cases. Torrance HW Glasgow Med J; 1922 May; 97(5):263-273. PubMed ID: 30437346 [No Abstract] [Full Text] [Related]
40. Tay-Sachs' Disease: A Study of the Symptomatology and Pathology of Three Atypical Cases. Torrance HW Glasgow Med J; 1922 Jun; 97(6):341-360. PubMed ID: 30437364 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]