Works matching Payne Stewart
Results: 20
THE IMPACT OF HOME SCHOOLING REGULATIONS ON EDUCATIONAL ENROLLMENTS IN THE UNITED STATES.
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- Education, 2005, v. 126, n. 2, p. 353
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- Article
Two novel polymorphisms (E277K and V212V) in the haemochromatosis gene HFE.
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- Human Mutation, 2000, v. 15, n. 1, p. 120, doi. 10.1002/(SICI)1098-1004(200001)15:1<120::AID-HUMU32>3.0.CO;2-B
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- Article
A novel missense mutation S65C in the HFE gene with a possible role in hereditary haemochromatosis.
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- Human Mutation, 1999, v. 13, n. 6, p. 507, doi. 10.1002/(SICI)1098-1004(1999)13:6<507::AID-HUMU25>3.0.CO;2-X
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- Article
Autistic-like behaviour profile and psychiatric morbidity in Fragile X Syndrome.
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- European Child & Adolescent Psychiatry, 2003, v. 12, n. 4, p. 172, doi. 10.1007/s00787-003-0333-3
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- Article
Development of a denaturing high-performance liquid chromatography screening method for SMAD4 in juvenile polyposis syndrome.
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- Annals of Clinical Biochemistry, 2007, v. 44, n. 2, p. 159, doi. 10.1258/000456307780118181
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- Article
The type of somatic mutation at APC in familial adenomatous polyposis is determined by the site of the germline mutation: a new facet to Knudson's 'two-hit' hypothesis.
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- Nature Medicine, 1999, v. 5, n. 9, p. 1071, doi. 10.1038/12511
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- Article
Female Germline Mosaicism in Tuberous Sclerosis Confirmed by Molecular Genetic Analysis.
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- Human Molecular Genetics, 1997, v. 6, n. 13, p. 2265, doi. 10.1093/hmg/6.13.2265
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- Article
A Family with Stickler Syndrome Type 2 Has a Mutation in the COL11A1 Gene Resulting in the Substitution of Glycine 97 by Valine in a1(XI) Collagen.
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- Human Molecular Genetics, 1996, v. 5, n. 9, p. 1339, doi. 10.1093/hmg/5.9.1339
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- Article
Molecular analysis of de novo germline mutations in the von Hippel-Lindau disease gene.
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- Human Molecular Genetics, 1995, v. 4, n. 11, p. 2139
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- Article
Molecular genetic analysis of the 3p — syndrome.
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- Human Molecular Genetics, 1994, v. 3, n. 6, p. 903
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- Article
Direct, non-radioactive detection of mutations in Multiple Endocrine Neoplasia Type 2A families.
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- Human Molecular Genetics, 1994, v. 3, n. 4, p. 643
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- Article
Clinical correlation and molecular evaluation confirm that the MLH1 p.Arg182Gly (c.544A>G) mutation is pathogenic and causes Lynch syndrome.
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- Familial Cancer, 2012, v. 11, n. 3, p. 509, doi. 10.1007/s10689-012-9544-4
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- Article
Gene-related cancer spectrum in families with hereditary non-polyposis colorectal cancer (HNPCC).
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- Familial Cancer, 2008, v. 7, n. 2, p. 163
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- Article
An individual with Muir-Torre syndrome found to have a pathogenic MSH6 gene mutation.
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- Familial Cancer, 2007, v. 6, n. 3, p. 317, doi. 10.1007/s10689-007-9119-y
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- Article
Contribution of cyclin d1 (CCND1) and E-cadherin (CDH1) polymorphisms to familial and sporadic colorectal cancer.
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- Oncogene, 2002, v. 21, n. 12, p. 1928, doi. 10.1038/sj.onc.1205245
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- Article
Chromosome 19p13.3 deletion in a patient with macrocephaly, obesity, mental retardation, and behavior problems.
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- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 5, p. 1192, doi. 10.1002/ajmg.a.33986
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- Article
Sir Wilfrid Laurier: The Weakling Who Stood His Ground.
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- 2006
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- Book Review
Women's Health.
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- 1998
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- Publication type:
- Book Review
Not Always Black and White: The Effect of Race and Emotional Expression on Implicit Attitudes.
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- Social Cognition, 2018, v. 36, n. 5, p. 534, doi. 10.1521/soco.2018.36.5.534
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- Article
Immediate affect as a basis for intuitive moral judgement: An adaptation of the affect misattribution procedure.
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- Cognition & Emotion, 2010, v. 24, n. 3, p. 522, doi. 10.1080/02699930902847193
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- Article