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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
The hemoglobinopathies and malaria.
- Published in:
- Clinical Genetics, 2005, v. 68, n. 4, p. 332, doi. 10.1111/j.1399-0004.2005.00503.x
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- Publication type:
- Article
Genetic landmarks through philately: Georges Marinesco (1863–1938).
- Published in:
- Clinical Genetics, 2003, v. 64, n. 4, p. 297, doi. 10.1034/j.1399-0004.2003.00158.x
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- Publication type:
- Article
History of genetics through philately – Carl Linnaeus (Carl von Linné).
- Published in:
- Clinical Genetics, 2001, v. 60, n. 2, p. 104, doi. 10.1034/j.1399-0004.2001.600203.x
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- Publication type:
- Article
Shakespeare as a geneticist.
- Published in:
- 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.
- Published in:
- Clinical Genetics, 2001, v. 59, n. 1, p. 25, doi. 10.1034/j.1399-0004.2001.590104.x
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- Publication type:
- Article
Genetic landmarks through philately – Thomas Hunt Morgan (1866–1945).
- Published in:
- 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.
- Published in:
- 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.
- Published in:
- 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
Hallowed beginning.
- Published in:
- 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 evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype.
- Published in:
- 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
Genetic landmarks through philately – Crick, Watson and Wilkins: the scientists behind DNA structure.
- Published in:
- 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.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 4, p. 279, doi. 10.1034/j.1399-0004.1999.560404.x
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- Publication type:
- Article
Genetic landmarks through philately – Kabuki theater and Kabuki syndrome.
- Published in:
- 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.
- Published in:
- 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.
- Published in:
- 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 - symbols in medicine.
- Published in:
- 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 – porphyria and its effect on world history.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 2, p. 85, doi. 10.1034/j.1399-0004.1999.550203.x
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- Article
Obituary.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 2, p. 135, doi. 10.1034/j.1399-0004.1999.550214.x
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- Publication type:
- Article
Genetic landmarks through philately - The Habsburg jaw.
- Published in:
- 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).
- Published in:
- 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
Response to Correspondence on “Lissencephaly With Brainstem and Cerebellar Hypoplasia and Congenital Cataracts”.
- Published in:
- 2015
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- Publication type:
- Letter to the Editor
Lissencephaly With Brainstem and Cerebellar Hypoplasia and Congenital Cataracts.
- Published in:
- 2014
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- Publication type:
- Case Study
Molecular characterization of 13 patients with PIK3CA‐related overgrowth spectrum using a targeted deep sequencing approach.
- Published in:
- American Journal of Medical Genetics. Part A, 2024, v. 194, n. 3, p. 1, doi. 10.1002/ajmg.a.63466
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- Publication type:
- Article
Classifications of split hand foot malformation (SHFM) should include transverse deficiencies: Why Maisels was correct.
- Published in:
- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 9, p. 2809, doi. 10.1002/ajmg.a.62242
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- Publication type:
- Article
Alternative genomic diagnoses for individuals with a clinical diagnosis of Dubowitz syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 1, p. 119, doi. 10.1002/ajmg.a.61926
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- Publication type:
- Article
The Coffin-Siris syndrome: A proposed diagnostic approach and assessment of 15 overlapping cases.
- Published in:
- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 8, p. 1865, doi. 10.1002/ajmg.a.35415
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- Publication type:
- Article
A shared founder mutation underlies restrictive dermopathy in Old Colony (Dutch-German) Mennonite and Hutterite patients in North America.
- Published in:
- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 5, p. 1229, doi. 10.1002/ajmg.a.35302
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- Publication type:
- Article
Risk factors for nonsyndromic holoprosencephaly: A Manitoba case-control study.
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- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 4, p. 751, doi. 10.1002/ajmg.a.35240
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- Publication type:
- Article
Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay.
- Published in:
- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 2, p. 391, doi. 10.1002/ajmg.a.34216
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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.
- Published in:
- Public Health Ethics, 2016, v. 9, n. 1, p. 65, doi. 10.1093/phe/phv012
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- Publication type:
- Article
Successful pregnancy following continuous treatment with combination chemotherapy before conception and throughout pregnancy.
- Published in:
- 1984
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- Publication type:
- journal 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
Fetal hepatic haemangioendothelioma: a new association with elevated maternal serum alpha-fetoprotein.
- Published in:
- 2000
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- Publication type:
- Case Study
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
Response to "A critique for the new Canadian FASD diagnostic Guidelines".
- Published in:
- Journal of the Canadian Academy of Child & Adolescent Psychiatry, 2018, v. 27, n. 2, p. 83
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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
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
Functional Evaluation of Hidden Figures Object Analysis in Children with Autistic Disorder.
- Published in:
- 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.
- Published in:
- 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.
- Published in:
- 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.
- Published in:
- 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
Meeting the needs of future physicians: a core curriculum initiative for postgraduate medical education at a Canadian university.
- Published in:
- Medical Education, 2001, v. 35, n. 10, p. 973, doi. 10.1046/j.1365-2923.2001.01021.x
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- Publication type:
- Article
Phyllis Jean McAlpine, Ph.D, FCCMG.
- Published in:
- 1998
- By:
- Publication type:
- Obituary
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
Infantile muscular dystrophy in Canadian aboriginals is an αB-crystallinopathy.
- Published in:
- 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
- By:
- Publication type:
- journal article
Fetal Alcohol Spectrum Disorder--High Rates, High Needs, High Time for Action.
- Published in:
- JAMA Pediatrics, 2017, v. 171, n. 10, p. 940, doi. 10.1001/jamapediatrics.2017.2232
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- Publication type:
- Article
Relationships between Head Circumference, Brain Volume and Cognition in Children with Prenatal Alcohol Exposure.
- Published in:
- PLoS ONE, 2016, v. 11, n. 2, p. 1, doi. 10.1371/journal.pone.0150370
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- Publication type:
- Article