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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1964 2
1968 1
1969 1
1970 3
1971 7
1972 2
1973 5
1974 3
1975 7
1976 2
1977 11
1978 7
1979 2
1980 3
1981 2
1982 5
1983 3
1984 1
1985 2
1987 3
1988 1
1989 1
1990 3
1992 3
1993 2
1994 1
1995 2
1997 2
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2001 4
2002 1
2004 1
2012 2
2014 1
2024 0

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98 results

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Page 1
Michael Kaback: people and places.
Kaback MM. Kaback MM. Genet Med. 2014 Dec;16(12):981-3. doi: 10.1038/gim.2014.44. Epub 2014 May 1. Genet Med. 2014. PMID: 24784159 Free article. No abstract available.
Future perspectives for Tay-Sachs disease.
Desnick RJ, Kaback MM. Desnick RJ, et al. Among authors: kaback mm. Adv Genet. 2001;44:349-56. doi: 10.1016/s0065-2660(01)44091-0. Adv Genet. 2001. PMID: 11596996 Review. No abstract available.
Infantile metachromatic leukodystrophy.
Kaback MM, Howell RR. Kaback MM, et al. N Engl J Med. 1970 Jun 11;282(24):1336-40. doi: 10.1056/NEJM197006112822403. N Engl J Med. 1970. PMID: 4192207 No abstract available.
Evaluation of mental retardation: recommendations of a Consensus Conference: American College of Medical Genetics.
Curry CJ, Stevenson RE, Aughton D, Byrne J, Carey JC, Cassidy S, Cunniff C, Graham JM Jr, Jones MC, Kaback MM, Moeschler J, Schaefer GB, Schwartz S, Tarleton J, Opitz J. Curry CJ, et al. Among authors: kaback mm. Am J Med Genet. 1997 Nov 12;72(4):468-77. doi: 10.1002/(sici)1096-8628(19971112)72:4<468::aid-ajmg18>3.0.co;2-p. Am J Med Genet. 1997. PMID: 9375733 Review.
Tay-Sachs screening: social and psychological impact.
Childs B, Gordis L, Kaback MM, Kazazian HH Jr. Childs B, et al. Among authors: kaback mm. Am J Hum Genet. 1976 Nov;28(6):550-8. Am J Hum Genet. 1976. PMID: 1032905 Free PMC article.
Inherited lipid storage diseases of the central nervous system.
Percy AK, Shapiro LJ, Kaback MM. Percy AK, et al. Among authors: kaback mm. Curr Probl Pediatr. 1979 Sep;9(11):1-51. doi: 10.1016/s0045-9380(79)80020-1. Curr Probl Pediatr. 1979. PMID: 117977 Review. No abstract available.
Eight novel mutations in the HEXA gene.
McGinniss MJ, Brown DH, Fulwiler A, Marten M, Lim-Steele JS, Kaback MM. McGinniss MJ, et al. Among authors: kaback mm. Genet Med. 2002 May-Jun;4(3):158-61. doi: 10.1097/00125817-200205000-00010. Genet Med. 2002. PMID: 12180151 Free article.
David L. Rimoin.
Cohn DH, Shapiro LJ, Kaback MM. Cohn DH, et al. Among authors: kaback mm. Am J Hum Genet. 2012 Sep 7;91(3):403-7. doi: 10.1016/j.ajhg.2012.08.001. Am J Hum Genet. 2012. PMID: 23240132 Free PMC article. No abstract available.
98 results