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Items: 1 to 20 of 23

1.

Genetic heterogeneity in human disease.

McClellan J, King MC.

Cell. 2010 Apr 16;141(2):210-7. doi: 10.1016/j.cell.2010.03.032.

2.

Selection and mutation in the "new" genetics: an emerging hypothesis.

Gottlieb B, Beitel LK, Alvarado C, Trifiro MA.

Hum Genet. 2010 Mar;127(5):491-501. doi: 10.1007/s00439-010-0792-9. Review.

PMID:
20099069
3.

Genetics of type II diabetes.

Permutt MA, Chiu K, Ferrer J, Glaser B, Inoue H, Nestorowicz A, Stanley CA, Tanizawa Y.

Recent Prog Horm Res. 1998;53:201-16. Review.

PMID:
9769709
4.

Genetic variation in ICF syndrome: evidence for genetic heterogeneity.

Wijmenga C, Hansen RS, Gimelli G, Björck EJ, Davies EG, Valentine D, Belohradsky BH, van Dongen JJ, Smeets DF, van den Heuvel LP, Luyten JA, Strengman E, Weemaes C, Pearson PL.

Hum Mutat. 2000 Dec;16(6):509-17. Review.

PMID:
11102980
5.

Common genetic variation and human disease.

Orr N, Chanock S.

Adv Genet. 2008;62:1-32. doi: 10.1016/S0065-2660(08)00601-9. Review.

PMID:
19010252
6.

Transthyretin mutations in health and disease.

Saraiva MJ.

Hum Mutat. 1995;5(3):191-6. Review.

PMID:
7599630
7.

[Disease-causing mutations versus neutral polymorphism: use of bioinformatics and DNA diagnosis].

Machácková E.

Cas Lek Cesk. 2003 Mar;142(3):150-3. Review. Czech.

PMID:
12756842
8.
9.

[Genetics of atrial fibrillation: rare mutations, common variants and clinical relevance?].

Sinner MF, Pfeufer A, Kääb S.

Herzschrittmacherther Elektrophysiol. 2006 Jun;17(2):95-105. Review. German.

PMID:
16786468
10.

Haplotype trees and modern human origins.

Templeton AR.

Am J Phys Anthropol. 2005;Suppl 41:33-59. Review.

PMID:
16369961
11.

Molecular abnormalities of FSH and LH action.

McDonough PG.

Ann N Y Acad Sci. 2003 Nov;997:22-34. Review.

PMID:
14644806
12.

Human cancer syndromes: clues to the origin and nature of cancer.

Fearon ER.

Science. 1997 Nov 7;278(5340):1043-50. Review.

PMID:
9353177
13.

Molecular genetics of arrhythmias--a new paradigm.

Schulze-Bahr E, Haverkamp W, Borggrefe M, Wedekind H, Mönnig G, Mergenthaler J, Assmann G, Funke H, Breithardt G.

Z Kardiol. 2000;89 Suppl 4:IV12-22. Review.

PMID:
10810773
14.

Emerging themes and new challenges in defining the role of structural variation in human disease.

Sharp AJ.

Hum Mutat. 2009 Feb;30(2):135-44. doi: 10.1002/humu.20843. Review.

PMID:
18837009
15.

Finding genes influencing susceptibility to complex diseases in the post-genome era.

Rannala B.

Am J Pharmacogenomics. 2001;1(3):203-21. Review.

PMID:
12083968
16.

Genetic variation analysis for biomedical researchers: a primer.

Barnes MR.

Methods Mol Biol. 2010;628:1-20. doi: 10.1007/978-1-60327-367-1_1. Review.

PMID:
20238073
17.

[Mechanisms and consequences of genetic mutations].

Vidaud M.

Rev Prat. 1997 Jan 15;47(2):146-54. Review. French.

PMID:
9157512
18.

Gene modifiers of lung disease.

Knowles MR.

Curr Opin Pulm Med. 2006 Nov;12(6):416-21. Review.

PMID:
17053491
19.
20.

Identical mutations and phenotypic variation.

Wolf U.

Hum Genet. 1997 Sep;100(3-4):305-21. Review.

PMID:
9272148
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