Hamerton JL - Search Results

1

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: hamerton jl. Am J Med Genet. 1990 Apr;35(4):536-45. doi: 10.1002/ajmg.1320350420. Am J Med Genet. 1990. PMID: 1970703

2

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: hamerton jl. Am J Med Genet. 1992 Jun 1;43(3):588-91. doi: 10.1002/ajmg.1320430316. Am J Med Genet. 1992. PMID: 1605253

3

Somatic recombination rather than uniparental disomy suggested as another mechanism by which genetic imprinting may play a role in the etiology of Prader-Willi syndrome.

Gregory CA, Schwartz J, Kirkilionis AJ, Rudd N, Hamerton JL. Gregory CA, et al. Among authors: hamerton jl. Hum Genet. 1991 Nov;88(1):42-8. doi: 10.1007/BF00204927. Hum Genet. 1991. PMID: 1683645

4

Molecular and clinical overlap of Angelman and Prader-Willi syndrome phenotypes.

Kirkilionis AJ, Chudley AE, Gregory CA, Hamerton JL. Kirkilionis AJ, et al. Among authors: hamerton jl. Am J Med Genet. 1991 Sep 15;40(4):454-9. doi: 10.1002/ajmg.1320400416. Am J Med Genet. 1991. PMID: 1684091

5

Long-range restriction mapping and linkage analysis of the Prader-Willi chromosome region (PWCR).

Kirkilionis AJ, Gregory CA, Hamerton JL. Kirkilionis AJ, et al. Among authors: hamerton jl. Genomics. 1991 Mar;9(3):524-35. doi: 10.1016/0888-7543(91)90420-j. Genomics. 1991. PMID: 2032723

6

The gene for prolactin-inducible protein (PIP), uniquely expressed in exocrine organs, maps to chromosome 7.

Myal Y, Gregory C, Wang H, Hamerton JL, Shiu RP. Myal Y, et al. Among authors: hamerton jl. Somat Cell Mol Genet. 1989 May;15(3):265-70. doi: 10.1007/BF01534877. Somat Cell Mol Genet. 1989. PMID: 2727805

7

Familial mental retardation in a family with an inherited chromosome rearrangement.

Chudley AE, Bauder F, Ray M, McAlpine PJ, Pena SD, Hamerton JL. Chudley AE, et al. Among authors: hamerton jl. J Med Genet. 1974 Dec;11(4):353-66. doi: 10.1136/jmg.11.4.353. J Med Genet. 1974. PMID: 4140909 Free PMC article.

8

Physical and psychological findings in adolescents with sex chromosome abnormalities ascertained in the Winnipeg Cytogenetic Study of Newborns: 1970-1973.

Evans JA, de von Flindt R, Greenberg CR, Hamerton JL. Evans JA, et al. Among authors: hamerton jl. Birth Defects Orig Artic Ser. 1990;26(4):189-99. Birth Defects Orig Artic Ser. 1990. PMID: 2090317 No abstract available.

9

TaqI and RsaI RFLP's at the prolactin inducible protein (PIP) locus on chromosome 7.

Myal Y, Gregory CA, Karpan C, Hamerton JL, Shiu RP. Myal Y, et al. Among authors: hamerton jl. Nucleic Acids Res. 1989 Jul 25;17(14):5879. doi: 10.1093/nar/17.14.5879. Nucleic Acids Res. 1989. PMID: 2569729 Free PMC article. No abstract available.

10

A BglII RFLP at the human prolactin gene locus on chromosome 6 (PRL).

Myal Y, DiMattia GE, Gregory CA, Friesen HG, Hamerton JL, Shiu RP. Myal Y, et al. Among authors: hamerton jl. Nucleic Acids Res. 1991 Mar 11;19(5):1167. doi: 10.1093/nar/19.5.1167-a. Nucleic Acids Res. 1991. PMID: 1673564 Free PMC article.

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