D. Allingham-Hawkins

发表

Prevalence and penetrance of BRCA1 and BRCA2 gene mutations in unselected Ashkenazi Jewish women with breast cancer.

W. Foulkes, E. Warner, W. Meschino, 1999, Journal of the National Cancer Institute.

Fragile X premutation is a significant risk factor for premature ovarian failure: the International Collaborative POF in Fragile X study--preliminary data.

W. Brown, P. Jacobs, D. Chitayat, 1999, American journal of medical genetics.

DecisionDx-GBM Gene Expression Assay for Prognostic Testing in Glioblastoma Multiform

D. Allingham-Hawkins, Andrew Lea, S. Levine, 2010, PLoS currents.

Tissue-specific methylation differences and cognitive function in fragile X premutation females.

D. Chitayat, D. Allingham-Hawkins, P. Ray, 1996, American journal of medical genetics.

BRAF p.Val600Glu (V600E) Testing for Assessment of Treatment Options in Metastatic Colorectal Cancer

D. Allingham-Hawkins, Andrew Lea, S. Levine, 2010, PLoS currents.

Impact of carrier status determination for Duchenne/Becker muscular dystrophy by computer-assisted laser densitometry.

D. Allingham-Hawkins, P. Ray, J. Sutherland, 1998, American journal of medical genetics.

KIF 6 p . Trp 719 Arg Testing to Assess Risk of Coronary Artery Disease and / or Statin Response November

D. Allingham-Hawkins, Andrew Lea, Susan Levine Allingham-Hawkins, 2016 .

KIF6 p.Trp719Arg Testing to Assess Risk of Coronary Artery Disease and/or Statin Response

D. Allingham-Hawkins, Andrew Lea, S. Levine, 2010, PLoS currents.

Regulation of Genetic Testing/Service in Canada

D. Allingham-Hawkins, M. Somerville, 2010 .

Eighth International workshop on the fragile X syndrome and X-linked mental retardation, August 16-22, 1997.

C. Gunter, C. Schwartz, W. Brown, 1999, American journal of medical genetics.

De novo chromosome 7q36.1q36.2 triplication in a child with developmental delay, growth failure, distinctive facial features, and multiple congenital anomalies: a case report

D. Allingham-Hawkins, A. El-Hattab, M. A. Al Dhaibani, 2017, BMC Medical Genetics.

Prospective validation of quantitative fluorescent polymerase chain reaction for rapid detection of common aneuploidies

D. Chitayat, D. Allingham-Hawkins, V. Cirigliano, 2011, Genetics in Medicine.

Heterogeneity in Roberts syndrome.

D. Allingham-Hawkins, D. Tomkins, 1995, American journal of medical genetics.

Somatic cell hybridization of roberts syndrome and normal lymphoblasts resulting in correction of both the cytogenetic and mutagen hypersensitivity cellular phenotypes

D. Allingham-Hawkins, D. Tomkins, 1991, Somatic cell and molecular genetics.

Predictive, pre‐natal and diagnostic genetic testing for Huntington's disease: the experience in Canada from 1987 to 2000

B. Fernandez, M. Hayden, W. Meschino, 2003, Clinical genetics.

Whole exome sequencing for cancer – is there evidence of clinical utility?

Alka Malhotra, Susan Levine, D. Allingham-Hawkins, 2014 .

Apparently unstable normal FMR1 alleles in nine developmentally delayed patients: implications for molecular diagnosis of the fragile X syndrome.

M. Somerville, D. Allingham-Hawkins, A. Summers, 2000, Genetic testing.

WDR45B‐related intellectual disability, spastic quadriplegia, epilepsy, and cerebral hypoplasia: A consistent neurodevelopmental syndrome

F. Alkuraya, D. Allingham-Hawkins, A. El-Hattab, 2018, Clinical genetics.

ERCC1 Expression Analysis to Guide Therapy in Non-Small Cell Lung Cancer

D. Allingham-Hawkins, Andrew Lea, S. Levine, 2010, PLoS currents.

Compound heterozygosity for the Achondroplasia-hypochondroplasia FGFR3 mutations: prenatal diagnosis and postnatal outcome.

B. Fernandez, D. Chitayat, D. Allingham-Hawkins, 1999, American journal of medical genetics.

Developmentally Delayed Males

D. Allingham-Hawkins, P. Ray, 2007 .

Vanishing endometrial carcinoma.

T. Colgan, S. Kamel‐Reid, D. Allingham-Hawkins, 2007, International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists.

FRAXE expansion is not a common etiological factor among developmentally delayed males.

D. Allingham-Hawkins, P. Ray, 1995, American journal of human genetics.

Canadian College of Medical Geneticists Canadian Association of Genetic Counsellors Joint Statement on the Process of Informed Consent for Genetic Research

D. Allingham-Hawkins, L. Cartier, T. Nelson, 2009 .

Expression of X-linked bulbospinal muscular atrophy (Kennedy disease) in two homozygous women.

B. Schmidt, D. Allingham-Hawkins, C. Greenberg, 2002, Neurology.

Prevalence and penetrance of BRCA1 and BRCA2 gene mutations in unselected Ashkenazi Jewish women with breast cancer.

W. Foulkes, E. Warner, W. Meschino, 1999, Journal of the National Cancer Institute.

Braf P.val600glu (v600e) Testing for Assessment of Treatment Options in Metastatic Colorectal Cancer Test Description

D. Allingham-Hawkins, Andrew Lea, S. Levine, 2022 .