Kusmartsev V, Drozdz M, Schuster-Bockler B, Warnecke T
Genetics. 2020; 214(4):809-823.
PMID: 32079595
PMC: 7153944.
DOI: 10.1534/genetics.120.303028.
Mizukami K, Raj K, Giger U
J Vet Intern Med. 2014; 29(1):120-5.
PMID: 25417848
PMC: 4858075.
DOI: 10.1111/jvim.12501.
Helentjaris T, King G, Slocum M, Siedenstrang C, Wegman S
Plant Mol Biol. 2013; 5(2):109-18.
PMID: 24306570
DOI: 10.1007/BF00020093.
Landry B, Kesseli R, Leung H, Michelmore R
Theor Appl Genet. 2013; 74(5):646-53.
PMID: 24240222
DOI: 10.1007/BF00288865.
McCouch S, Kochert G, Yu Z, Wang Z, Khush G, Coffman W
Theor Appl Genet. 2013; 76(6):815-29.
PMID: 24232389
DOI: 10.1007/BF00273666.
RFLP-based genetic maps of wheat homoeologous group 7 chromosomes.
Chao S, Sharp P, Worland A, Warham E, Koebner R, Gale M
Theor Appl Genet. 2013; 78(4):495-504.
PMID: 24225676
DOI: 10.1007/BF00290833.
DNA variation in tissue-culture-derived rice plants.
Muller E, Brown P, Hartke S, Lorz H
Theor Appl Genet. 2013; 80(5):673-9.
PMID: 24221075
DOI: 10.1007/BF00224228.
Copy-number variation: the balance between gene dosage and expression in Drosophila melanogaster.
Zhou J, Lemos B, Dopman E, Hartl D
Genome Biol Evol. 2011; 3:1014-24.
PMID: 21979154
PMC: 3227403.
DOI: 10.1093/gbe/evr023.
Gradual transition from mosaic to global DNA methylation patterns during deuterostome evolution.
Okamura K, Matsumoto K, Nakai K
BMC Bioinformatics. 2010; 11 Suppl 7:S2.
PMID: 21106124
PMC: 2957685.
DOI: 10.1186/1471-2105-11-S7-S2.
Clinical outcomes in Menkes disease patients with a copper-responsive ATP7A mutation, G727R.
Tang J, Donsante A, Desai V, Patronas N, Kaler S
Mol Genet Metab. 2008; 95(3):174-81.
PMID: 18752978
PMC: 2654537.
DOI: 10.1016/j.ymgme.2008.06.015.
Marked variation in predicted and observed variability of tandem repeat loci across the human genome.
ODushlaine C, Shields D
BMC Genomics. 2008; 9:175.
PMID: 18416815
PMC: 2364633.
DOI: 10.1186/1471-2164-9-175.
Fabry disease: identification of 50 novel alpha-galactosidase A mutations causing the classic phenotype and three-dimensional structural analysis of 29 missense mutations.
Shabbeer J, Yasuda M, Benson S, Desnick R
Hum Genomics. 2006; 2(5):297-309.
PMID: 16595074
PMC: 3500179.
DOI: 10.1186/1479-7364-2-5-297.
Nav1.5/R1193Q polymorphism is associated with both long QT and Brugada syndromes.
Huang H, Zhao J, Barrane F, Champagne J, Chahine M
Can J Cardiol. 2006; 22(4):309-13.
PMID: 16568155
PMC: 2560523.
DOI: 10.1016/s0828-282x(06)70915-1.
Combined deficiency of factor V and factor VIII is due to mutations in either LMAN1 or MCFD2.
Zhang B, McGee B, Yamaoka J, Guglielmone H, Downes K, Minoldo S
Blood. 2005; 107(5):1903-7.
PMID: 16304051
PMC: 1895703.
DOI: 10.1182/blood-2005-09-3620.
Relationship between X-inactivation and clinical involvement in Fabry heterozygotes. Eleven novel mutations in the alpha-galactosidase A gene in the Czech and Slovak population.
Dobrovolny R, Dvorakova L, Ledvinova J, Magage S, Bultas J, Lubanda J
J Mol Med (Berl). 2005; 83(8):647-54.
PMID: 15806320
DOI: 10.1007/s00109-005-0656-2.
Identification of an angiogenic factor that when mutated causes susceptibility to Klippel-Trenaunay syndrome.
Tian X, Kadaba R, You S, Liu M, Timur A, Yang L
Nature. 2004; 427(6975):640-5.
PMID: 14961121
PMC: 1618873.
DOI: 10.1038/nature02320.
A rheostat model for a rapid and reversible form of imprinting-dependent evolution.
Beaudet A, Jiang Y
Am J Hum Genet. 2002; 70(6):1389-97.
PMID: 11992247
PMC: 379123.
DOI: 10.1086/340969.
Identification and expression of mutations in the hydroxymethylbilane synthase gene causing acute intermittent porphyria (AIP).
Solis C, Astrin K, Desnick R
Mol Med. 1999; 5(10):664-71.
PMID: 10602775
PMC: 2230478.
X-linked adrenoleukodystrophy: genes, mutations, and phenotypes.
Smith K, Kemp S, Braiterman L, Lu J, Wei H, Geraghty M
Neurochem Res. 1999; 24(4):521-35.
PMID: 10227685
DOI: 10.1023/a:1022535930009.
A systematic approach for detecting high-frequency restriction fragment length polymorphisms using large genomic probes.
Feder J, Yen L, Wijsman E, Wang L, Wilkins L, Schroder J
Am J Hum Genet. 1985; 37(4):635-49.
PMID: 9556655
PMC: 1684621.