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Dietary Intake Patterns and Lifestyle Behaviors of Pregnant Women Living in a Manitoba First Nations Community: Implications for Fetal Alcohol Spectrum Disorder.
- Published in:
- Nutrients, 2022, v. 14, n. 15, p. 3233, doi. 10.3390/nu14153233
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- Publication type:
- Article
Possible association of rare autosomal folate sensitive fragile sites and idiopathic mental retardation: a blind controlled population study.
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- Clinical Genetics, 1990, v. 38, n. 4, p. 241, doi. 10.1111/j.1399-0004.1990.tb03577.x
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- Publication type:
- Article
Infantile muscular dystrophy in Canadian aboriginals is an αB-crystallinopathy.
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- Annals of Neurology, 2011, v. 69, n. 5, p. 866, doi. 10.1002/ana.22331
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- Publication type:
- Article
Infantile muscular dystrophy in Canadian aboriginals is an αB-crystallinopathy.
- Published in:
- 2011
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- Publication type:
- journal article
Risk and Resilience Variants in the Retinoic Acid Metabolic and Developmental Pathways Associated with Risk of FASD Outcomes.
- Published in:
- Biomolecules (2218-273X), 2024, v. 14, n. 5, p. 569, doi. 10.3390/biom14050569
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- Publication type:
- Article
Meeting the needs of future physicians: a core curriculum initiative for postgraduate medical education at a Canadian university.
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- Medical Education, 2001, v. 35, n. 10, p. 973, doi. 10.1046/j.1365-2923.2001.01021.x
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- Article
The hemoglobinopathies and malaria.
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- Clinical Genetics, 2005, v. 68, n. 4, p. 332, doi. 10.1111/j.1399-0004.2005.00503.x
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- Article
Genetic landmarks through philately: Georges Marinesco (1863–1938).
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- Clinical Genetics, 2003, v. 64, n. 4, p. 297, doi. 10.1034/j.1399-0004.2003.00158.x
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- Article
History of genetics through philately – Carl Linnaeus (Carl von Linné).
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- Clinical Genetics, 2001, v. 60, n. 2, p. 104, doi. 10.1034/j.1399-0004.2001.600203.x
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- Article
Shakespeare as a geneticist.
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- Clinical Genetics, 2001, v. 59, n. 3, p. 165, doi. 10.1034/j.1399-0004.2001.590304.x
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- Publication type:
- Article
Grebe syndrome in Vietnamese sisters: not Agent Orange.
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- Clinical Genetics, 2001, v. 59, n. 1, p. 25, doi. 10.1034/j.1399-0004.2001.590104.x
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- Article
Genetic landmarks through philately – Thomas Hunt Morgan (1866–1945).
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- Clinical Genetics, 2000, v. 58, n. 1, p. 25
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- Publication type:
- Article
Genetic landmarks through philately – Jean Martin Charcot (1825–1893) and Charcot–Marie–Tooth disease.
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- Clinical Genetics, 2000, v. 57, n. 6, p. 420, doi. 10.1034/j.1399-0004.2000.570603.x
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- Publication type:
- Article
Genetic landmarks through philately – Karl Landsteiner: the father of blood grouping.
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- Clinical Genetics, 2000, v. 57, n. 4, p. 267, doi. 10.1034/j.1399-0004.2000.570404.x
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- Publication type:
- Article
Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype.
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- Clinical Genetics, 2000, v. 57, n. 2, p. 103, doi. 10.1034/j.1399-0004.2000.570203.x
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- Publication type:
- Article
Hallowed beginning.
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- Clinical Genetics, 2000, v. 57, n. 2, p. 101, doi. 10.1034/j.1399-0004.2000.570202.x
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- Publication type:
- Article
Genetic landmarks through philately – Crick, Watson and Wilkins: the scientists behind DNA structure.
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- Clinical Genetics, 2000, v. 57, n. 1, p. 26, doi. 10.1034/j.1399-0004.2000.570104.x
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- Publication type:
- Article
Genetic landmarks through philately – hemophilia.
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- Clinical Genetics, 1999, v. 56, n. 4, p. 279, doi. 10.1034/j.1399-0004.1999.560404.x
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- Article
Genetic landmarks through philately – Kabuki theater and Kabuki syndrome.
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- Clinical Genetics, 1999, v. 56, n. 2, p. 116, doi. 10.1034/j.1399-0004.1999.560203.x
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- Publication type:
- Article
Genetic landmarks through philately – hereditary breast cancer1.
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- Clinical Genetics, 1999, v. 55, n. 6, p. 416, doi. 10.1034/j.1399-0004.1999.550604.x
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- Publication type:
- Article
Genetic landmarks through philately – a brief history of diabetes mellitus.
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- Clinical Genetics, 1999, v. 55, n. 4, p. 231, doi. 10.1034/j.1399-0004.1999.550403.x
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- Publication type:
- Article
Genetic landmarks through philately – porphyria and its effect on world history.
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- Clinical Genetics, 1999, v. 55, n. 2, p. 85, doi. 10.1034/j.1399-0004.1999.550203.x
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- Article
Obituary.
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- Clinical Genetics, 1999, v. 55, n. 2, p. 135, doi. 10.1034/j.1399-0004.1999.550214.x
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- Article
Genetic landmarks through philately - symbols in medicine.
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- Clinical Genetics, 1998, v. 54, n. 6, p. 474, doi. 10.1111/j.1399-0004.1998.tb03767.x
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- Publication type:
- Article
Genetic landmarks through philately - The Habsburg jaw.
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- Clinical Genetics, 1998, v. 54, n. 4, p. 283, doi. 10.1111/j.1399-0004.1998.tb03729.x
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- Publication type:
- Article
Genetic landmarks through philately - Gregor Johann Mendel (1822-1884).
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- Clinical Genetics, 1998, v. 54, n. 2, p. 121, doi. 10.1111/j.1399-0004.1998.tb03713.x
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- Publication type:
- Article
Genetics and cardiac anomalies: the heart of the matter.
- Published in:
- 2002
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- Publication type:
- journal article
Fetal hepatic haemangioendothelioma: a new association with elevated maternal serum alpha-fetoprotein.
- Published in:
- 2000
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- Publication type:
- case study
DNA methylation as a predictor of fetal alcohol spectrum disorder.
- Published in:
- Clinical Epigenetics, 2018, v. 10, p. 1, doi. 10.1186/s13148-018-0439-6
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- Publication type:
- Article
Functional Evaluation of Hidden Figures Object Analysis in Children with Autistic Disorder.
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- Journal of Autism & Developmental Disorders, 2011, v. 41, n. 1, p. 13, doi. 10.1007/s10803-010-1013-z
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- Publication type:
- Article
2p15-p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders.
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- European Journal of Human Genetics, 2011, v. 19, n. 12, p. 1264, doi. 10.1038/ejhg.2011.112
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- Publication type:
- Article
The DLX1and DLX2 genes and susceptibility to autism spectrum disorders.
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- European Journal of Human Genetics, 2009, v. 17, n. 2, p. 228, doi. 10.1038/ejhg.2008.148
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- Publication type:
- Article
Mutation in the 5'alternatively spliced region of the XNP/ATR-X gene causes Chudley-Lowry syndrome.
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- European Journal of Human Genetics, 2005, v. 13, n. 2, p. 176, doi. 10.1038/sj.ejhg.5201303
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- Publication type:
- Article
Increased Nuchal Translucency Thickness: A Potential Indicator for Ritscher-Schinzel Syndrome.
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- Fetal Diagnosis & Therapy, 2008, v. 24, n. 4, p. 395, doi. 10.1159/000165697
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- Publication type:
- Article
Fetal Alcohol Spectrum Disorder--High Rates, High Needs, High Time for Action.
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- JAMA Pediatrics, 2017, v. 171, n. 10, p. 940, doi. 10.1001/jamapediatrics.2017.2232
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- Publication type:
- Article
It's a Shame! Stigma Against Fetal Alcohol Spectrum Disorder: Examining the Ethical Implications for Public Health Practices and Policies.
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- Public Health Ethics, 2016, v. 9, n. 1, p. 65, doi. 10.1093/phe/phv012
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- Publication type:
- Article
A global research collaboration on fetal alcohol spectrum disorder.
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- Biochemistry & Cell Biology, 2018, v. 96, n. 2, p. vii, doi. 10.1139/bcb-2018-0088
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- Publication type:
- Article
Copy number variation in fetal alcohol spectrum disorder.
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- Biochemistry & Cell Biology, 2018, v. 96, n. 2, p. 161, doi. 10.1139/bcb-2017-0241
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- Publication type:
- Article
Diagnosis of fetal alcohol spectrum disorder: current practices and future considerations.
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- Biochemistry & Cell Biology, 2018, v. 96, n. 2, p. 231, doi. 10.1139/bcb-2017-0106
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- Publication type:
- Article
Autosomal recessive cerebellar hypoplasia in the Hutterite population.
- Published in:
- 2005
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- Publication type:
- journal article
Autosomal recessive cerebellar hypoplasia in the Hutterite population.
- Published in:
- Developmental Medicine & Child Neurology, 2005, v. 47, n. 10, p. 691, doi. 10.1017/S0012162205001404
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- Publication type:
- Article
Response to "A critique for the new Canadian FASD diagnostic Guidelines".
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- Journal of the Canadian Academy of Child & Adolescent Psychiatry, 2018, v. 27, n. 2, p. 83
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- Publication type:
- Article
Cost of Fetal Alcohol Spectrum Disorder Diagnosis in Canada.
- Published in:
- PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0060434
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- Publication type:
- Article
Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis.
- Published in:
- Nature Genetics, 2007, v. 39, n. 8, p. 1018, doi. 10.1038/ng2072
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- Publication type:
- Article
Profile of Mothers of Children with Fetal Alcohol Spectrum Disorder: A Population-Based Study in Canada.
- Published in:
- International Journal of Environmental Research & Public Health, 2020, v. 17, n. 21, p. 7986, doi. 10.3390/ijerph17217986
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- Publication type:
- Article
Fetal alcohol spectrum disorder: a guideline for diagnosis across the lifespan.
- Published in:
- 2016
- By:
- Publication type:
- journal article
A G-to-T transversion at the +5 position of intron 1 in the glutaryl CoA dehydrogenase gene is associated with the island Lake variant of glutaric acidemia type I.
- Published in:
- Human Molecular Genetics, 1995, v. 4, n. 3, p. 493
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- Publication type:
- Article
DNA methylation signature of human fetal alcohol spectrum disorder.
- Published in:
- Epigenetics & Chromatin, 2016, v. 9, p. 1, doi. 10.1186/s13072-016-0074-4
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- Publication type:
- Article
Prevalence of Pervasive Developmental Disorders in Two Canadian Provinces.
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- Journal of Policy & Practice in Intellectual Disabilities, 2006, v. 3, n. 3, p. 164, doi. 10.1111/j.1741-1130.2006.00076.x
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- Publication type:
- Article
Are FASD guidelines practical and sustainable?
- Published in:
- 2005
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- Publication type:
- Letter