P W Allderdice
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Explore the profile of P W Allderdice including associated specialties, affiliations and a list of published articles.
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Articles
41
Citations
454
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Recent Articles
1.
Allderdice P, Woodland B, Allderdice W
Can Fam Physician
. 2011 Jan;
33:162-6.
PMID: 21267350
Family physicians are at the frontier in health promotion. They have opportunity to identify many familial genetic risks prior to health crises. Early diagnosis allows time to discuss choices: schedules...
2.
Allderdice P, OLeary E, Ficken S
Can Fam Physician
. 2011 Jan;
34:849-970.
PMID: 21253090
Family physicians uncover clues to genetic risk while they routinely sketch and add to patients' genograms. A symbolic international language identifies health conditions and shows inter- and intra-generational relationships of...
3.
Galutira D, Allderdice P, Davidson W
Nucleic Acids Res
. 1991 Dec;
19(23):6667.
PMID: 1684431
No abstract available.
4.
Allderdice P, Gardner H, Galutira D, Lockridge O, LADU B, McAlpine P
Genomics
. 1991 Oct;
11(2):452-4.
PMID: 1769657
Human tissues have two distinct cholinesterase activities: acetylcholinesterase and butyrylcholinesterase. Acetylcholinesterase functions in the transmission of nerve impulses, whereas the physiological function of butyryl-cholinesterase remains unknown. An atypical form of...
5.
McAlpine P, Dixon M, Allderdice P, Lockridge O, La Du B
Nucleic Acids Res
. 1991 Sep;
19(18):5088.
PMID: 1717941
No abstract available.
6.
Allderdice P, Ali M, McAlpine P
Am J Med Genet
. 1991 Jun;
39(4):396-8.
PMID: 1877616
The first example known to us of complementation by two non-homologous chromosomes 3 is present in the karyotype of a phenotypically normal brother of an inv(3)(p25q21) carrier. The normal chromosomes...
7.
PHILIPPS S, Kaita H, Lewis M, Allderdice P
Gene Geogr
. 1988 Aug;
2(2-3):133-9.
PMID: 3154132
Data are presented on 30 high and low incidence antigens and on the distribution of the alleles of 14 blood group systems in a random sample of Newfoundlanders. The distribution...
8.
Allderdice P, Kaita H, Lewis M, McAlpine P, Wong P, Anderson J, et al.
Am J Hum Genet
. 1986 Nov;
39(5):612-7.
PMID: 3024483
Cytogenetic, enzyme dosage, serological, and electrophoretic analyses of blood samples from members of three Newfoundland kindreds in which one specific paracentric insertion chromosome inv ins(9)(q22.1q34.3q34.1) is segregating provide data indicating...
9.
Ross J, Allderdice P, Shapiro L, Aveling J, Eales B, Simms Jr D
Arch Dermatol
. 1985 Dec;
121(12):1524-8.
PMID: 3864397
Steroid sulfatase (STS)-deficient X-linked ichthyosis was diagnosed in a man with short stature and mental retardation. His generation includes five similarly affected male members. A translocation chromosome is segregating in...
10.
Lewis M, Kaita H, Allderdice P, Bergren M, McAlpine P
Hum Genet
. 1984 Jan;
67(3):270-1.
PMID: 6336320
A "new" low incidence red cell antigen, NFLD, is described. It was found in a Caucasian family and is inherited as an autosomal dominant. The antigen is not part of...