Isolation of a cDNA encoding the human G_M2 activator proteinSCHRÖDER, M; KLIMA, H; NAKANO, T et al.FEBS letters. 1989, Vol 251, Num 1-2, pp 197-200, issn 0014-5793, 4 p.Article

A new form of residual hexosaminidase activity in infantile Tay Sachs disease fibroblastsHECHTMAN, P; KHOO, K; ISAACS, C et al.Clinical genetics. 1983, Vol 24, Num 3, pp 206-215, issn 0009-9163Article

The mutation mechanism causing juvenile-onset Tay-Sachs disease among LebaneseHECHTMAN, P; BOULAY, B; BAYLERAN, J et al.Clinical genetics. 1989, Vol 35, Num 5, pp 364-375, issn 0009-9163, 12 p.Article

TAY-SACHS AND RELATED STORAGE DISEASES: FAMILY PLANNING.SCHNEIDERMAN G; LOWDEN JA; RAE GRANT P et al.1978; MENTAL RETARDAT.; U.S.A.; DA. 1978; VOL. 16; NO 1; PP. 13-15; BIBL. 11 REF.Article

A pseudodeficiency allele common inn non-jewish Tay-Sachs carriers : implications for carrier screeningTRIGGS-RAINE, B. L; MULES, E. H; GREENBERG, C. R et al.American journal of human genetics. 1992, Vol 51, Num 4, pp 793-801, issn 0002-9297Article

Characterization of some minor gangliosides in Tay-Sachs brainsYU, R. K; ITOH, T; YOHE, H. C et al.Brain research. 1983, Vol 275, Num 1, pp 47-52, issn 0006-8993Article

Late onset G_M2 gangliosidosis: an α-locus genetic compound with near normal hexosaminidase activityCHARROW, J; INUI, K; WENGER, D. A et al.Clinical genetics. 1985, Vol 27, Num 1, pp 78-84, issn 0009-9163Article

Prenatal diagnosis of Tay-Sachs disease. Reflectometry of hexosaminidase A, B, and C/S bands on zymogramsKUSTERMANN-KUHN, B; HARZER, K.Human genetics. 1983, Vol 65, Num 2, pp 172-175, issn 0340-6717Article

Pitfalls in Tay-Sachs carrier detection: physician referral patterns and patient ignoranceSHAPIRO, D. A; SHAPIRO, L. R.New York State journal of medicine. 1989, Vol 89, Num 6, pp 317-319, issn 0028-7628, 3 p.Article

LA MALADIE DE TAY-SACHS: A PROPOS DE DEUX OBSERVATIONS DANS DES FAMILLES BRETONNESCASTEL Y; TOUDIC L; PARENT P et al.1982; REV. INT. PEDIATR.; ISSN 0048-8135; FRA; DA. 1982; NO 119; PP. 41-54; 10 P.; ABS. ENG; BIBL. 10 REF.Article

RETINAL AMACRINE CELL INVOLVEMENT IN TAY-SACHS DISEASENAGASHIMA K; KIKUCHI F; SUZUKI Y et al.1981; ACTA NEUROPATHOL.; ISSN 0001-6322; DEU; DA. 1981; VOL. 53; NO 4; PP. 333-336; BIBL. 22 REF.Article

NORMAL ADULT WITH ABSENT HEX A: IMMUNOREACTIVE HEX A IS PRESENTO'BRIEN JS; GEIGER B.1979; AMER. J. HUM. GENET.; USA; DA. 1979; VOL. 31; NO 5; PP. 642-646; BIBL. 16 REF.Article

ROLE OF GENETIC DRIFT IN THE HIGH FREQUENCY OF TAY-SACHS DISEASE AMONG ASHKENAZIC JEWSYOKOYAMA S.1979; ANN. HUM. GENET.; GBR; DA. 1979; VOL. 43; NO 2; PP. 133-136; BIBL. 12 REF.Article

ELEVATED FREQUENCY OF TAY-SACHS DISEASE AMONG ASHKENAZIC JEWS UNLIKELY BY GENETIC DRIFT ALONE.CHAKRAVARTI A; CHAKRABORTY R.1978; AMER. J. HUM. GENET.; USA; DA. 1978; VOL. 30; NO 3; PP. 256-261; BIBL. 15 REF.Article

UNADJUSTED CARRIER FREQUENCY FOR COMMUNITY SCREENING PROGRAMS.CORSON VL; KAZAZIAN HH JR.1978; AMER. J. HUM. GENET.; U.S.A.; DA. 1978; VOL. 30; NO 2; PP. 227; BIBL. 2 REF.Article

HEALTH BEHAVIOR AND GENETIC SCREENING FOR CARRIERS OF TAY-SACHS DISEASE: A PROSPECTIVE STUDY.GOLDSTEIN MS; GREENWALD S; NATHAN T et al.1977; SOC. SCI. MED.; G.B.; DA. 1977; VOL. 11; NO 8-9; PP. 515-520; BIBL. 9 REF.Article

MALADIE DE TAY-SACHS ET ANESTHESIE: UN CASMASUKO K; TAKEDA N; SHIMOJI K et al.1977; JAP. J. ANESTHESIOL.; JAP.; DA. 1977; VOL. 26; NO 2; PP. 183-189; ABS. ANGL.; BIBL. 1 P. 1/2Article

LOW LEVELS OF BETA HEXOSAMINIDASE A IN HEALTHY INDIVIDUALS WITH APPARENT DEFICIENCY OF THIS ENZYME.NAVON R; GEIGER B; BEN YOSEPH Y et al.1976; AMER. J. HUM. GENET.; U.S.A.; DA. 1976; VOL. 28; NO 4; PP. 339-349; BIBL. 1 P. 1/2Article

HETEROZYGOTE ADVANTAGE IN TAY-SACHS CARRIERS.SPYROPOULOS B; MOENS PB; DAVIDSON J et al.1981; AM. J. HUM. GENET.; ISSN 0002-9297; USA; DA. 1981; VOL. 33; NO 3; PP. 375-380; BIBL. 17 REF.Article

AN ECONOMIC EVALUATION OF A GENETIC SCREENING PROGRAM FOR TAY-SACHS DISEASE.NELSON WB; SWINT JM; CASKEY CT et al.1978; AMER. J. HUM. GENET.; U.S.A.; DA. 1978; VOL. 30; NO 2; PP. 160-166; BIBL. 13 REF.Article

KNOWLEDGE ABOUT AND ATTITUDES TOWARD GENETIC SCREENING AMONG HIGH-SCHOOL STUDENTS: THE TAY-SACHS EXPERIENCE.CLOW CL; SCRIVER CR.1977; PEDIATRICS; U.S.A.; DA. 1977; VOL. 59; NO 1; PP. 86-91; BIBL. 10 REF.Article

TAY-SACHS DISEASE AND CARRIER SCREENING PROGRAMS: PSYCHOSOCIAL ASPECTS.SCHNEIDERMAN G; LOWDEN JA; RAE GRANT Q et al.1977; CANAD. J. PUBLIC HEALTH; CANADA; DA. 1977; VOL. 68; NO 1; PP. 66-68; ABS. FR.; BIBL. 12 REF.Article

ADVOCACY AND COMPLIANCE FACTORS IN A VOLUNTARY SELECTIVE SCREENING PROGRAM.ROTHSCHILD H; IVKER FB.1977; SOUTH. MED. J.; U.S.A.; DA. 1977; VOL. 70; NO 2; PP. 184-186; BIBL. 19 REF.Article

TAY-SACHS DISEASE: A PILOT SCREENING PROGRAM FOR THE DETECTION OF THE HETEROZYGOTE IN THE CHARLESTON JEWISH COMMUNITY.ROGERS JF; HOGAN EL; JORGENSON RJ et al.1976; SOUTH. MED. J.; U.S.A.; DA. 1976; VOL. 69; NO 11; PP. 1453-1455; BIBL. 8 REF.Article

TAY-SACHS SCREENING: MOTIVES FOR PARTICIPATING AND KNOWLEDGE OF GENETICS AND PROBABILITY.CHILDS B; GORDIS L; KABACK MM et al.1976; AMER. J. HUM. GENET.; U.S.A.; DA. 1976; VOL. 28; NO 6; PP. 537-549; BIBL. 10 REF.Article