Gregory CA - Search Results

1

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: gregory ca. Genomics. 1991 Mar;9(3):524-35. doi: 10.1016/0888-7543(91)90420-j. Genomics. 1991. PMID: 2032723

2

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. Hum Genet. 1991 Nov;88(1):42-8. doi: 10.1007/BF00204927. Hum Genet. 1991. PMID: 1683645

3

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: gregory ca. Am J Med Genet. 1991 Sep 15;40(4):454-9. doi: 10.1002/ajmg.1320400416. Am J Med Genet. 1991. PMID: 1684091

4

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

5

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. Somat Cell Mol Genet. 1989 May;15(3):265-70. doi: 10.1007/BF01534877. Somat Cell Mol Genet. 1989. PMID: 2727805

6

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: gregory ca. 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.

7

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: gregory ca. 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.

8

Assignment of human glutaryl-CoA dehydrogenase gene (GCDH) to the short arm of chromosome 19 (19p13.2) by in situ hybridization and somatic cell hybrid analysis.

Greenberg CR, Duncan AM, Gregory CA, Singal R, Goodman SI. Greenberg CR, et al. Among authors: gregory ca. Genomics. 1994 May 1;21(1):289-90. doi: 10.1006/geno.1994.1264. Genomics. 1994. PMID: 8088809 No abstract available.

9

RFLPs are detected by two probes isolated by chromosome walking from pTD3-21 (D15S10) which maps to 15q11.2-12.

Gregory CA, Schwartz JS. Gregory CA, et al. Nucleic Acids Res. 1991 Apr 11;19(7):1726. doi: 10.1093/nar/19.7.1726-a. Nucleic Acids Res. 1991. PMID: 1674145 Free PMC article. No abstract available.

10

The cDNA of the human neuromedin B gene (NMB) mapped to 15q11-qter recognizes an XbaI RFLP.

Gregory CA, Schwartz JS. Gregory CA, et al. Nucleic Acids Res. 1991 Mar 11;19(5):1167. doi: 10.1093/nar/19.5.1167. Nucleic Acids Res. 1991. PMID: 1673565 Free PMC article.

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