Greenberg CR - Search Results

1

Predictive testing for Huntington disease in Canada: adverse effects and unexpected results in those receiving a decreased risk.

Huggins M, Bloch M, Wiggins S, Adam S, Suchowersky O, Trew M, Klimek M, Greenberg CR, Eleff M, Thompson LP, et al. Huggins M, et al. Among authors: greenberg cr. Am J Med Genet. 1992 Feb 15;42(4):508-15. doi: 10.1002/ajmg.1320420417. Am J Med Genet. 1992. PMID: 1535178

2

Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm.

Telenius H, Kremer B, Goldberg YP, Theilmann J, Andrew SE, Zeisler J, Adam S, Greenberg C, Ives EJ, Clarke LA, et al. Telenius H, et al. Nat Genet. 1994 Apr;6(4):409-14. doi: 10.1038/ng0494-409. Nat Genet. 1994. PMID: 8054984

3

Predictive, pre-natal and diagnostic genetic testing for Huntington's disease: the experience in Canada from 1987 to 2000.

Creighton S, Almqvist EW, MacGregor D, Fernandez B, Hogg H, Beis J, Welch JP, Riddell C, Lokkesmoe R, Khalifa M, MacKenzie J, Sajoo A, Farrell S, Robert F, Shugar A, Summers A, Meschino W, Allingham-Hawkins D, Chiu T, Hunter A, Allanson J, Hare H, Schween J, Collins L, Sanders S, Greenberg C, Cardwell S, Lemire E, MacLeod P, Hayden MR. Creighton S, et al. Clin Genet. 2003 Jun;63(6):462-75. doi: 10.1034/j.1399-0004.2003.00093.x. Clin Genet. 2003. PMID: 12786753

4

Three years' experience with neonatal screening for Duchenne/Becker muscular dystrophy: gene analysis, gene expression, and phenotype prediction.

Greenberg CR, Jacobs HK, Halliday W, Wrogemann K. Greenberg CR, et al. Am J Med Genet. 1991 Apr 1;39(1):68-75. doi: 10.1002/ajmg.1320390115. Am J Med Genet. 1991. PMID: 1867267

5

Molecular analysis of juvenile Huntington disease: the major influence on (CAG)n repeat length is the sex of the affected parent.

Telenius H, Kremer HP, Theilmann J, Andrew SE, Almqvist E, Anvret M, Greenberg C, Greenberg J, Lucotte G, Squitieri F, et al. Telenius H, et al. Hum Mol Genet. 1993 Oct;2(10):1535-40. doi: 10.1093/hmg/2.10.1535. Hum Mol Genet. 1993. PMID: 8268906

6

Germline E-cadherin mutations in hereditary diffuse gastric cancer: assessment of 42 new families and review of genetic screening criteria.

Brooks-Wilson AR, Kaurah P, Suriano G, Leach S, Senz J, Grehan N, Butterfield YS, Jeyes J, Schinas J, Bacani J, Kelsey M, Ferreira P, MacGillivray B, MacLeod P, Micek M, Ford J, Foulkes W, Australie K, Greenberg C, LaPointe M, Gilpin C, Nikkel S, Gilchrist D, Hughes R, Jackson CE, Monaghan KG, Oliveira MJ, Seruca R, Gallinger S, Caldas C, Huntsman D. Brooks-Wilson AR, et al. J Med Genet. 2004 Jul;41(7):508-17. doi: 10.1136/jmg.2004.018275. J Med Genet. 2004. PMID: 15235021 Free PMC article.

7

Novel and recurrent mutations in lamin A/C in patients with Emery-Dreifuss muscular dystrophy.

Brown CA, Lanning RW, McKinney KQ, Salvino AR, Cherniske E, Crowe CA, Darras BT, Gominak S, Greenberg CR, Grosmann C, Heydemann P, Mendell JR, Pober BR, Sasaki T, Shapiro F, Simpson DA, Suchowersky O, Spence JE. Brown CA, et al. Among authors: greenberg cr. Am J Med Genet. 2001 Sep 1;102(4):359-67. doi: 10.1002/ajmg.1463. Am J Med Genet. 2001. PMID: 11503164

8

Transmission of the fra(X) haplotype from three nonpenetrant brothers to their affected grandsons.

Kirkilionis AJ, Chudley AE, Greenberg CR, Yan DL, McGillivray B, Hamerton JL. Kirkilionis AJ, et al. Among authors: greenberg cr. Am J Med Genet. 1992 Jun 1;43(3):588-91. doi: 10.1002/ajmg.1320430316. Am J Med Genet. 1992. PMID: 1605253

9

Impact of genetic counselling after neonatal screening for Duchenne muscular dystrophy.

Hildes E, Jacobs HK, Cameron A, Seshia SS, Booth F, Evans JA, Wrogemann K, Greenberg CR. Hildes E, et al. Among authors: greenberg cr. J Med Genet. 1993 Aug;30(8):670-4. doi: 10.1136/jmg.30.8.670. J Med Genet. 1993. PMID: 8411054 Free PMC article.

10

Detection of molecular rearrangements in Prader-Willi syndrome patients by using genomic probes recognizing four loci within the PWCR.

Gregory CA, Kirkilionis AJ, Greenberg CR, Chudley AE, Hamerton JL. Gregory CA, et al. Among authors: greenberg cr. Am J Med Genet. 1990 Apr;35(4):536-45. doi: 10.1002/ajmg.1320350420. Am J Med Genet. 1990. PMID: 1970703

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