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Items: 1 to 50 of 150

1.

Defining the chromosomal basis of mental handicap.

Hamerton JL, Stranc L.

Lancet. 1999 Nov 13;354(9191):1659-60. No abstract available.

PMID:
10568562
2.

Chorionic villus sampling and amniocentesis for prenatal diagnosis.

Stranc LC, Evans JA, Hamerton JL.

Lancet. 1997 Mar 8;349(9053):711-4. Review. No abstract available.

PMID:
9078211
3.

Limb defects and chorionic villus sampling.

Evans JA, Hamerton JL.

Lancet. 1996 Feb 24;347(9000):484-5. No abstract available.

PMID:
8596260
4.

Prenatal diagnosis in Canada--1990: a review.

Stranc LC, Evans JA, Hamerton JL.

Prenat Diagn. 1994 Dec;14(13):1253-65. Review.

PMID:
7617571
5.

Chromosomal localization of a sequence with in vivo activity for initiation of DNA replication.

Shihab-el-Deen A, Wu C, Hamerton JL, Zannis-Hadjopoulos M, Price GB.

Somat Cell Mol Genet. 1993 Jan;19(1):103-9.

PMID:
8460395
6.

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.

Am J Med Genet. 1992 Jun 1;43(3):588-91.

PMID:
1605253
7.

Familial chromosomal aberrations and metabolic disorders.

Hamerton JL, Dallaire L, Tomkins D, Lippman A.

Prenat Diagn. 1992 May;12(5):473-6. No abstract available.

PMID:
1523213
8.

Canadian multicentre randomized clinical trial of chorion villus sampling and amniocentesis. Final report.

Lippman A, Tomkins DJ, Shime J, Hamerton JL.

Prenat Diagn. 1992 May;12(5):385-408. No abstract available.

PMID:
1523206
9.
10.

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

Kirkilionis AJ, Chudley AE, Gregory CA, Hamerton JL.

Am J Med Genet. 1991 Sep 15;40(4):454-9.

PMID:
1684091
11.

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.

Nucleic Acids Res. 1991 Mar 11;19(5):1167. No abstract available.

12.

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

Kirkilionis AJ, Gregory CA, Hamerton JL.

Genomics. 1991 Mar;9(3):524-35.

PMID:
2032723
13.

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.

Am J Med Genet. 1990 Apr;35(4):536-45.

PMID:
1970703
14.

The human X chromosome.

Hamerton JL.

Birth Defects Orig Artic Ser. 1990;26(4):283-7. Review. No abstract available.

PMID:
2090326
15.

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.

Birth Defects Orig Artic Ser. 1990;26(4):189-99. No abstract available.

PMID:
2090317
16.

Sex chromosome anomalies: prenatal diagnosis and the need for continued prospective studies.

Evans JA, MacDonald K, Hamerton JL.

Birth Defects Orig Artic Ser. 1990;26(4):273-81. No abstract available.

PMID:
1708684
17.

Chromosomal localization and structure of the human P1 protamine gene.

Krawetz SA, Herfort MH, Hamerton JL, Pon RT, Dixon GH.

Genomics. 1989 Oct;5(3):639-45.

PMID:
2613245
18.

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.

Nucleic Acids Res. 1989 Jul 25;17(14):5879. No abstract available.

19.

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.

Somat Cell Mol Genet. 1989 May;15(3):265-70.

PMID:
2727805
20.

Localization of the gene encoding human factor V to chromosome 1q21-25.

Wang H, Riddell DC, Guinto ER, MacGillivray RT, Hamerton JL.

Genomics. 1988 May;2(4):324-8.

PMID:
3220473
21.

Structural gene encoding human factor XII is located at 5q33-qter.

Royle NJ, Nigli M, Cool D, MacGillivray RT, Hamerton JL.

Somat Cell Mol Genet. 1988 Mar;14(2):217-21.

PMID:
3162339
22.

Confirmation of the assignment of MYCL to chromosome 1 in humans and its position relative to RH, UMPK, and PGM1.

Zelinski T, Verville G, White L, Hamerton JL, McAlpine PJ, Lewis M.

Genomics. 1988 Feb;2(2):154-6.

PMID:
2842250
23.
24.

Isolation and characterization of a processed gene for human ceruloplasmin.

Koschinsky ML, Chow BK, Schwartz J, Hamerton JL, MacGillivray RT.

Biochemistry. 1987 Dec 1;26(24):7760-7.

PMID:
3427102
25.

DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21.

Greenberg CR, Hamerton JL, Nigli M, Wrogemann K.

Am J Hum Genet. 1987 Aug;41(2):128-37.

26.

Human genes encoding prothrombin and ceruloplasmin map to 11p11-q12 and 3q21-24, respectively.

Royle NJ, Irwin DM, Koschinsky ML, MacGillivray RT, Hamerton JL.

Somat Cell Mol Genet. 1987 May;13(3):285-92.

PMID:
3474786
27.

Two RFLPs identified by an anonymous sequence (D7S19) (pTS119) from chromosome 7.

Starr T, Wood S, Riddell DC, Hamerton JL.

Nucleic Acids Res. 1987 Mar 25;15(6):2784. No abstract available.

28.

Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy.

Kunkel LM, Hejtmancik JF, Caskey CT, Speer A, Monaco AP, Middlesworth W, Colletti CA, Bertelson C, Müller U, Bresnan M, Shapiro F, Tantravahi U, Speer J, Latt SA, Bartlett R, Pericak-Vance MA, Roses AD, Thompson MW, Ray PN, Worton RG, Fischbeck KH, Gallano P, Coulon M, Duros C, Boue J, Junien C, Chelly J, Hamard G, Jeanpierre M, Lambert M, Kaplan JC, Emery A, Dorkins H, McGlade S, Davies KE, Boehm C, Arveiler B, Lemaire C, Morgan GJ, Denton MJ, Amos J, Bobrow M, Benham F, Boswinkel E, Cole C, Dubowitz V, Hart K, Hodgson S, Johnson L, Walker A, Roncuzzi L, Ferlini A, Nobile C, Romeo G, Wilcox DE, Affara NA, Ferguson-Smith MA, Lindolf M, Kaariainen H, de la Chapelle A, Ionasescu V, Searby C, Ionasescu R, Bakker E, van Ommen GJ, Pearson PL, Greenberg CR, Hamerton JL, Wrogemann K, Doherty RA, Polakowska R, Hyser C, Quirk S, Thomas N, Harper JF, Darras BT, Francke U.

Nature. 1986 Jul 3-9;322(6074):73-7.

PMID:
3014348
29.

The characteristics of a population of Canadian women offered maternal serum alphafetoprotein screening during pregnancy.

Evans JA, MacDonald K, Hamerton JL.

Can J Public Health. 1986 May-Jun;77 Suppl 1:150-6. No abstract available.

PMID:
2427177
30.

Physical and psychologic parameters in children with sex chromosome anomalies: further follow-up from the Winnipeg Cytogenetic Study of 14,069 newborn infants.

Evans JA, de von Flindt R, Greenberg C, Ramsay S, Hamerton JL.

Birth Defects Orig Artic Ser. 1986;22(3):183-207. No abstract available.

PMID:
3814776
31.

Isolation and characterization of an alpha-satellite repeated sequence from human chromosome 22.

McDermid HE, Duncan AM, Higgins MJ, Hamerton JL, Rector E, Brasch KR, White BN.

Chromosoma. 1986;94(3):228-34.

PMID:
3769652
32.

The gene for clotting factor 10 is mapped to 13q32----qter.

Royle NJ, Fung MR, MacGillivray RT, Hamerton JL.

Cytogenet Cell Genet. 1986;41(3):185-8.

PMID:
3754199
33.

Regional localization of 18 human X-linked DNA sequences.

Riddell DC, Wang HS, Beckett J, Chan A, Holden JJ, Mulligan LM, Phillips MA, Simpson NE, Wrogemann K, Hamerton JL, et al.

Cytogenet Cell Genet. 1986;42(3):123-8.

PMID:
3460742
34.

A DNA marker for human chromosome 8 that detects alleles of differing sizes.

Wood S, Poon R, Riddell DC, Royle NJ, Hamerton JL.

Cytogenet Cell Genet. 1986;42(3):113-8.

PMID:
3460741
35.

Chromosomal assignment of human sequences encoding arginine vasopressin-neurophysin II and growth hormone releasing factor.

Riddell DC, Mallonee R, Phillips JA, Parks JS, Sexton LA, Hamerton JL.

Somat Cell Mol Genet. 1985 Mar;11(2):189-95.

PMID:
2984790
36.

Cytogenetic disorders.

Hamerton JL.

N Engl J Med. 1984 Feb 2;310(5):314-6. No abstract available.

PMID:
6690955
37.

Report of the Committee on the Genetic Constitution of Chromosome 1.

Hamerton JL, Povey S, Morton NE.

Cytogenet Cell Genet. 1984;37(1-4):3-21. Review. No abstract available.

PMID:
6360562
38.

56K fibroblast protein not specific for Duchenne muscular dystrophy but for skin biopsy site.

Thompson RG, Nickel B, Finlayson S, Meuser R, Hamerton JL, Wrogemann K.

Nature. 1983 Aug 25-31;304(5928):740-1.

PMID:
6888542
39.

Clonal culture of human amniocytes.

Hamerton JL.

Am J Med Genet. 1982 Nov;13(3):351. No abstract available.

PMID:
7180883
40.

Proline incorporation by cultured skin fibroblasts from patients with duchenne muscular dystrophy.

Thompson RG, Sponder ES, Rosenmann E, Hamerton JL, Wrogemann K.

J Neurol Sci. 1982 Nov-Dec;57(1):41-54.

PMID:
7153783
42.

Analysis of fibroblast proteins from patients with Duchenne muscular dystrophy by two-dimensional gel electrophoresis.

Rosenmann E, Kreis C, Thompson RG, Dobbs M, Hamerton JL, Wrogemann K.

Nature. 1982 Aug 5;298(5874):563-5.

PMID:
10465679
43.

Homozygous Robertsonian translocations in a fetus with 44 chromosomes.

Rockman-Greenberg C, Ray M, Evans JA, Canning N, Hamerton JL.

Hum Genet. 1982;61(3):181-4.

PMID:
7173858
44.

A cytogenetic survey of 14,069 newborn infants. IV. Further follow-up on the children with sex chromosome anomalies.

Evans JA, de von Flindt R, Greenberg C, Ramsay S, Hamerton JL.

Birth Defects Orig Artic Ser. 1982;18(4):169-84.

PMID:
7159717
45.
46.

Human chromosomes control growth of human-Chinese hamster somatic cell hybrids.

Donald LJ, Wang HS, Hamerton JL.

Somatic Cell Genet. 1982 Jan;8(1):105-13.

PMID:
7101100
47.

A ribulose 5-phosphate 3-epimerase (RPE) locus is on human chromosome 2.

Donald LJ, Wang HS, Hamerton JL.

Cytogenet Cell Genet. 1982;33(3):261-3. No abstract available.

PMID:
6957283
48.

Report of the committee on the genetic constitution of chromosome 1.

Cook PJ, Hamerton JL.

Birth Defects Orig Artic Ser. 1982;18(2):111-20. No abstract available.

PMID:
6891611
49.

The effects of gamma irradiation of human fibroblasts on human/Chinese hamster somatic cell hybrids.

Donald LJ, Wang HS, Holliday NJ, Hamerton JL.

Can J Genet Cytol. 1981;23(3):505-11.

PMID:
7332875

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