Works matching IS 00034800 AND DT 2007 AND VI 71 AND IP 6
Results: 16
Sample Size Needed to Detect Gene-Gene Interactions Using Linkage Analysis.
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- Annals of Human Genetics, 2007, v. 71, n. 6, p. 828, doi. 10.1111/j.1469-1809.2007.00367.x
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- Article
Interleukin 6 Variable Number of Tandem Repeats (VNTR) Gene Polymorphism in Centenarians.
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- Annals of Human Genetics, 2007, v. 71, n. 6, p. 843, doi. 10.1111/j.1469-1809.2007.00368.x
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- Article
Founder Effect of the 669insA Mutation in BSCL2 Gene Causing Berardinelli-Seip Congenital Lipodystrophy in a Cluster from Brazil.
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- Annals of Human Genetics, 2007, v. 71, n. 6, p. 729, doi. 10.1111/j.1469-1809.2007.00369.x
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- Article
Variation in 5' Promoter Region of the APOE gene Contributes to Predicting Ischemic Heart Disease (IHD) in the Population at Large: the Copenhagen City Heart Study.
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- Annals of Human Genetics, 2007, v. 71, n. 6, p. 762, doi. 10.1111/j.1469-1809.2007.00370.x
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- Article
Migration Rates and Genetic Structure of two Hungarian Ethnic Groups in Transylvania, Romania.
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- Annals of Human Genetics, 2007, v. 71, n. 6, p. 791, doi. 10.1111/j.1469-1809.2007.00371.x
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Association of Microsatellite Polymorphisms of the Human 14q13.2 Region with Type 2 Diabetes Mellitus in Latvian and Finnish Populations.
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- Annals of Human Genetics, 2007, v. 71, n. 6, p. 772, doi. 10.1111/j.1469-1809.2007.00372.x
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- Article
Fatal Malonyl CoA Decarboxylase Deficiency Due to Maternal Uniparental Isodisomy of the Telomeric End of Chromosome 16.
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- Annals of Human Genetics, 2007, v. 71, n. 6, p. 705, doi. 10.1111/j.1469-1809.2007.00373.x
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- Article
Persistence of the Common Hartnup Disease D173.
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- Annals of Human Genetics, 2007, v. 71, n. 6, p. 755, doi. 10.1111/j.1469-1809.2007.00375.x
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Leukocyte cDNA Analysis of NSD1 Derived from Confirmed Sotos Syndrome Patients.
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- Annals of Human Genetics, 2007, v. 71, n. 6, p. 713, doi. 10.1111/j.1469-1809.2007.00376.x
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- Article
The Impact of BRCA1 on Spina Bifida Meningomyelocele Lesions.
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- Annals of Human Genetics, 2007, v. 71, n. 6, p. 719, doi. 10.1111/j.1469-1809.2007.00377.x
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- Article
A Novel Approach to Detect Parent-of-Origin Effects from Pedigree Data with Application to Beckwith-Wiedemann Syndrome.
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- Annals of Human Genetics, 2007, v. 71, n. 6, p. 804, doi. 10.1111/j.1469-1809.2007.00378.x
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- Article
Fine Mapping of Disease Genes Using Tagging SNPs.
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- Annals of Human Genetics, 2007, v. 71, n. 6, p. 815, doi. 10.1111/j.1469-1809.2007.00379.x
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Mitochondrial and Y Chromosome Diversity in the English-Speaking Caribbean.
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- Annals of Human Genetics, 2007, v. 71, n. 6, p. 782, doi. 10.1111/j.1469-1809.2007.00380.x
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- Article
Sex-Specific Effects of AGT-6 and ACE I/D on Pulse Pressure After 6 Months on Antihypertensive Treatment: The GenHAT Study.
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- Annals of Human Genetics, 2007, v. 71, n. 6, p. 735, doi. 10.1111/j.1469-1809.2007.00381.x
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Evaluation of the Thyroid Transcription Factor-1 Gene ( TITF1) as a Hirschsprung's Disease Locus.
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- Annals of Human Genetics, 2007, v. 71, n. 6, p. 746, doi. 10.1111/j.1469-1809.2007.00384.x
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- Article
No Association of the ACTN3 Gene R577X Polymorphism with Endurance Performance in Ironman Triathlons.
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- Annals of Human Genetics, 2007, v. 71, n. 6, p. 777, doi. 10.1111/j.1469-1809.2006.00385.x
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- Article