111 related articles for article (PubMed ID: 10160221)
1. Browsing Mendel's library: appreciating the enormous heterogeneity of human genomes.
Kita MW
J Insur Med; 1995-1996 Winter; 27(3):188-97. PubMed ID: 10160221
[No Abstract] [Full Text] [Related]
2. Approaches to identify genes for complex human diseases: lessons from Mendelian disorders.
Dean M
Hum Mutat; 2003 Oct; 22(4):261-74. PubMed ID: 12955713
[TBL] [Abstract][Full Text] [Related]
3. [Molecular-genetic heterogeneity of hereditary diseases].
Gaĭtskhoki VS
Vopr Med Khim; 1997; 43(5):290-300. PubMed ID: 9446319
[TBL] [Abstract][Full Text] [Related]
4. Linkage analysis with gene-environment interaction: model illustration and performance of ordered subset analysis.
Schmidt S; Schmidt MA; Qin X; Martin ER; Hauser ER
Genet Epidemiol; 2006 Jul; 30(5):409-22. PubMed ID: 16671105
[TBL] [Abstract][Full Text] [Related]
5. The search for genenotype/phenotype associations and the phenome scan.
Jones R; Pembrey M; Golding J; Herrick D
Paediatr Perinat Epidemiol; 2005 Jul; 19(4):264-75. PubMed ID: 15958149
[TBL] [Abstract][Full Text] [Related]
6. A strategy for the rapid discovery of disease markers using the MassARRAY system.
Rodi CP; Darnhofer-Patel B; Stanssens P; Zabeau M; van den Boom D
Biotechniques; 2002 Jun; Suppl():62-6, 68-9. PubMed ID: 12083400
[No Abstract] [Full Text] [Related]
7. [Genetically based diseases].
González-Lamuño D; García Fuentes M
An Sist Sanit Navar; 2008; 31 Suppl 2():105-26. PubMed ID: 18953375
[TBL] [Abstract][Full Text] [Related]
8. Monogenic renal diseases: a clinical introduction.
Grünfeld JP
J Nephrol; 2002; 15 Suppl 6():S43-6. PubMed ID: 12515373
[TBL] [Abstract][Full Text] [Related]
9. [Genetic heterogeneity and phenotypic variability of hereditary diseases. 2].
Gencík A
Vnitr Lek; 1977 Sep; 23(9):840-8. PubMed ID: 919359
[No Abstract] [Full Text] [Related]
10. What Mendel did not discover: exceptions in Mendelian genetics and their role in inherited human disease.
Hern LM; Bidichandani SI
J Okla State Med Assoc; 2004 Jan; 97(1):12-7. PubMed ID: 14998061
[TBL] [Abstract][Full Text] [Related]
11. Modelling genotype-phenotype relationships and human disease with genetic interaction networks.
Lehner B
J Exp Biol; 2007 May; 210(Pt 9):1559-66. PubMed ID: 17449820
[TBL] [Abstract][Full Text] [Related]
12. [Genetic approaches to the study of human chronic diseases].
Bochkov NP; Ginter EK
Ter Arkh; 1981; 53(11):3-6. PubMed ID: 7339900
[No Abstract] [Full Text] [Related]
13. Yeast, flies, worms, and fish in the study of human disease.
Hariharan IK; Haber DA
N Engl J Med; 2003 Jun; 348(24):2457-63. PubMed ID: 12802034
[No Abstract] [Full Text] [Related]
14. The cypriot and Iranian National Mutation Frequency Databases.
Kleanthous M; Patsalis PC; Drousiotou A; Motazacker M; Christodoulou K; Cariolou M; Baysal E; Khrizi K; Moghimi B; Pourfarzad F; van Baal S; Deltas C; Najmabadi H; Patrinos GP
Hum Mutat; 2006 Jun; 27(6):598-9. PubMed ID: 16705699
[TBL] [Abstract][Full Text] [Related]
15. [Desperately seeking heritability].
Jordan B
Med Sci (Paris); 2010 May; 26(5):541-3. PubMed ID: 20510158
[No Abstract] [Full Text] [Related]
16. Phenome connections.
Oti M; Huynen MA; Brunner HG
Trends Genet; 2008 Mar; 24(3):103-6. PubMed ID: 18243400
[TBL] [Abstract][Full Text] [Related]
17. Phenogenetic drift and the evolution of genotype-phenotype relationships.
Weiss KM; Fullerton SM
Theor Popul Biol; 2000 May; 57(3):187-95. PubMed ID: 10828213
[No Abstract] [Full Text] [Related]
18. [Genetic heterogeneity of multifactorial diseases].
Crux-Coke R
Rev Med Chil; 1984 Oct; 112(10):1052-6. PubMed ID: 6536081
[No Abstract] [Full Text] [Related]
19. Genotype-phenotype comparison of the Swiss malignant hyperthermia population.
Girard T; Urwyler A; Censier K; Mueller CR; Zorzato F; Treves S
Hum Mutat; 2001 Oct; 18(4):357-8. PubMed ID: 11668625
[TBL] [Abstract][Full Text] [Related]
20. Epialleles and common disease.
Peedicayil J
Med Hypotheses; 2005; 64(1):215. PubMed ID: 15533644
[No Abstract] [Full Text] [Related]
[Next] [New Search]