B C McGillivray
Overview
Explore the profile of B C McGillivray including associated specialties, affiliations and a list of published articles.
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Articles
42
Citations
331
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Recent Articles
1.
McGillivray B
Can Fam Physician
. 2011 Jan;
32:2149-52.
PMID: 21267316
Genetic concerns and indications for prenatal diagnosis are first recognized by the family physician. Review of personal, pregnancy and family history may indicate concerns beyond that of advanced maternal age....
2.
McGillivray B
Can Fam Physician
. 2011 Jan;
34:895-8.
PMID: 21253096
Non-invasive modalities to assess the ongoing pregnancy may assist the clinician to identify risk factors requiring additions or alteration to routine prenatal care. These modalities include pedigree analysis, maternal serum...
3.
Schrader K, Nelson T, De Luca A, Huntsman D, McGillivray B
Clin Genet
. 2008 Dec;
75(2):185-9.
PMID: 19054014
We report a patient with a clinical and molecular diagnosis of LEOPARD syndrome (LS) associated with multiple granular cell tumors (MGCT). Bidirectional sequencing of exons 7, 12, and 13 of...
4.
Bajdik C, Raboud J, Schechter M, McGillivray B, Gallagher R
Math Biosci
. 2001 Apr;
171(1):99-111.
PMID: 11325386
The BRCA1 gene and its relationship to family history of breast/ovarian cancer are difficult to study in a population because of practical and ethical issues. The paucity of information on...
5.
Broadway D, Lyons C, McGillivray B
J AAPOS
. 1999 Oct;
2(3):188-90.
PMID: 10532759
A child born with partial trisomy of chromosome 1 (1q32-qter) survived and was seen for anterior segment dysgenesis and congenital glaucoma. Pure trisomy 1q is rarely seen in live-born infants...
6.
Cohen T, ZEITUNE M, McGillivray B, Hall J, Lynn A, Aston C, et al.
Am J Med Genet
. 1996 Oct;
65(3):226-34.
PMID: 9240749
Microcephaly is a heterogeneous disorder with genetic and environmental causes. However, there is little information on what proportion of cases are caused by inherited susceptibility, or the mode of inheritance...
7.
Drumheller T, McGillivray B, Behrner D, Macleod P, McFadden D, Roberson J, et al.
J Med Genet
. 1996 Oct;
33(10):842-7.
PMID: 8933338
In patients with the 3p-syndrome, hemizygous deletion of 3p25-pter is associated with profound growth failure, characteristic facial features, and mental retardation. We performed a molecular genetic analysis of 3p25 breakpoints...
8.
Choy F, Wei C, Applegarth D, McGillivray B
Am J Med Genet
. 1994 Jun;
51(2):156-60.
PMID: 7916532
Gaucher disease is the most frequent lysosomal lipid storage disease. It results from deficient glucocerebrosidase activity and is transmitted as an autosomal recessive trait. Three clinical forms of Gaucher disease...
9.
Van Allen M, Kalousek D, Chernoff G, Juriloff D, Harris M, McGillivray B, et al.
Am J Med Genet
. 1993 Oct;
47(5):723-43.
PMID: 8267004
Four separate initiation sites for neural tube (NT) fusion have been demonstrated recently in mice and other experimental animals. We evaluated the question of whether the multisite model vs. the...
10.
McGillivray B
Semin Perinatol
. 1992 Dec;
16(6):365-8.
PMID: 1293740
The unexpectedness of genital ambiguity in an infant creates an urgent and stressful situation. A logical approach, using a team of specialists together with nursery staff and physicians, allows each...