Kaback MM - Search Results

1

Screening and prevention in Tay-Sachs disease: origins, update, and impact.

Kaback MM. Kaback MM. Adv Genet. 2001;44:253-65. doi: 10.1016/s0065-2660(01)44084-3. Adv Genet. 2001. PMID: 11596988 No abstract available.

2

Tay-Sachs disease: from clinical description to molecular defect.

Kaback MM, Desnick RJ. Kaback MM, et al. Adv Genet. 2001;44:1-9. doi: 10.1016/s0065-2660(01)44065-x. Adv Genet. 2001. PMID: 11596975 No abstract available.

3

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.

4

Population-based genetic screening for reproductive counseling: the Tay-Sachs disease model.

Kaback MM. Kaback MM. Eur J Pediatr. 2000 Dec;159 Suppl 3:S192-5. doi: 10.1007/pl00014401. Eur J Pediatr. 2000. PMID: 11216898

5

Tay-Sachs disease--carrier screening, prenatal diagnosis, and the molecular era. An international perspective, 1970 to 1993. The International TSD Data Collection Network.

Kaback M, Lim-Steele J, Dabholkar D, Brown D, Levy N, Zeiger K. Kaback M, et al. JAMA. 1993 Nov 17;270(19):2307-15. JAMA. 1993. PMID: 8230592

6

Frequency of three Hex A mutant alleles among Jewish and non-Jewish carriers identified in a Tay-Sachs screening program.

Paw BH, Tieu PT, Kaback MM, Lim J, Neufeld EF. Paw BH, et al. Among authors: kaback mm. Am J Hum Genet. 1990 Oct;47(4):698-705. Am J Hum Genet. 1990. PMID: 2220809 Free PMC article.

7

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.

8

Tay-Sachs disease: high gene frequency in a non-Jewish population.

Kelly TE, Chase GA, Kaback MM, Kumor K, McKusick VA. Kelly TE, et al. Among authors: kaback mm. Am J Hum Genet. 1975 May;27(3):287-91. Am J Hum Genet. 1975. PMID: 803011 Free PMC article.

9

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.

10

The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%.

Oddoux C, Struewing JP, Clayton CM, Neuhausen S, Brody LC, Kaback M, Haas B, Norton L, Borgen P, Jhanwar S, Goldgar D, Ostrer H, Offit K. Oddoux C, et al. Nat Genet. 1996 Oct;14(2):188-90. doi: 10.1038/ng1096-188. Nat Genet. 1996. PMID: 8841192

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