J E Allanson
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Explore the profile of J E Allanson including associated specialties, affiliations and a list of published articles.
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Articles
47
Citations
707
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Recent Articles
1.
Hammond P, Forster-Gibson C, Chudley A, Allanson J, Hutton T, Farrell S, et al.
Mol Psychiatry
. 2008 Mar;
13(6):614-23.
PMID: 18317467
The heterogeneity of autism spectrum disorders (ASDs) confounds attempts to identify causes and pathogenesis. Identifiable endophenotypes and reliable biomarkers within ASDs would help to focus molecular research and uncover genetic...
2.
Armour C, Allanson J
J Med Genet
. 2007 Nov;
45(4):249-54.
PMID: 18039946
Background: Cardio-facio-cutaneous syndrome (CFC) is a multiple congenital anomaly/mental retardation syndrome named because of a characteristic facies, cardiac anomalies, and ectodermal abnormalities. While considerable literature describes the main features, few...
3.
Wszolek Z, Baba Y, Mackenzie I, Uitti R, Strongosky A, Broderick D, et al.
Neurology
. 2006 Aug;
67(4):620-5.
PMID: 16924015
Objective: To report genealogic, clinical, imaging, neuropathologic, and genetic data from a Canadian kindred with dystonia and brain calcinosis originally described in 1985. Methods: The authors performed clinical examinations and...
4.
Hunter A, Cappelli M, Humphreys L, Allanson J, Chiu T, Peeters C, et al.
Clin Genet
. 2005 Mar;
67(4):303-13.
PMID: 15733266
Prenatal diagnosis (PND) is offered routinely as part of pregnancy care to a large number of women at increased risk of fetal anomalies. Despite an extraordinary growth in the use...
5.
Ward R, Jamison P, Allanson J
Am J Med Genet
. 2000 Apr;
91(1):8-17.
PMID: 10751082
We have two objectives in this study: to demonstrate the utility of two summary anthropometric measures for quantifying craniofacial variation and to explore some of their potential uses by physicians...
6.
Graham G, Allanson J
Am J Med Genet
. 1999 Aug;
86(1):20-6.
PMID: 10440824
We describe a 14-month-old girl with unilateral congenital cholesteatoma and anomalies of the facial nerve in addition to the more common branchial arch, otic, and renal malformations comprising the branchio-oto-renal...
7.
Allanson J, GREENBERG F, Smith A
J Med Genet
. 1999 Jun;
36(5):394-7.
PMID: 10353786
We report a study of 55 subjects with Smith-Magenis syndrome, aged 9 months to 35 years. Each person has been evaluated with an assessment of "gestalt" and detailed facial measurement,...
8.
Allanson J, Ledbetter D, Dobyns W
J Med Genet
. 1998 Dec;
35(11):920-3.
PMID: 9832039
Both Miller-Dieker syndrome and isolated lissencephaly sequence are associated with classical lissencephaly. Both have been shown to be associated with deletions and mutations in LIS1 on 17p. Traditionally, the two...
9.
10.
Blumenthal A, Allanson J
Clin Genet
. 1997 Oct;
52(3):187-91.
PMID: 9377811
A patient with mosaic Turner syndrome and normal fertility had three documented pregnancies. She had a 45,X/46,X,r(X) karyotype and did not undergo spontaneous sexual maturation and menarche. Conception occurred while...