Works matching IS 14712350 AND DT 2012 AND VI 13 AND IP 1

Results: 124

Leukotriene B<sub>4</sub> receptor locus gene characterisation and association studies in asthma.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 1, doi. 10.1186/1471-2350-13-110

By:

Tulah, Asif S.;
Beghé, Bianca;
Barton, Sheila J.;
Holloway, John W.;
Sayers, Ian

Publication type:

Article

Evaluation of single nucleotide polymorphisms in microRNAs (hsa-miR-196a2 rs11614913 C/T) from Brazilian women with breast cancer.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 1, doi. 10.1186/1471-2350-13-119

By:

Linhares, José Juvenal;
Azevedo, Marcos;
Siufi, Adalberto Abraão;
de Carvalho, Cristina Valleta;
Garcia Molina Wolgien, Maria Del Carmen;
Noronha, Emmanuelle Coelho;
de Souza Bonetti, Tatiana Carvalho;
da Silva, Ismael Dale Cotrim Guerreiro

Publication type:

Article

Prediction of lung cancer risk in a Chinese population using a multifactorial genetic model.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 1, doi. 10.1186/1471-2350-13-118

By:

Huan Li;
Lixin Yang;
Xueying Zhao;
Jiucun Wang;
Ji Qian;
Hongyan Chen;
Weiwei Fan;
Hongcheng Liu;
Li Jin;
Weimin Wang;
Daru Lu

Publication type:

Article

In-vitro characterization of novel and functional regulatory SNPs in the promoter region of IL2 and IL2R alpha in a Gabonese population.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 1, doi. 10.1186/1471-2350-13-117

By:

Huang, Xiangsheng;
Kühne, Vera;
Kun, Jürgen .F J.;
Soboslay, Peter T.;
Lell, Bertrand;
Velavan, T. P.

Publication type:

Article

Thymic stromal lymphopoietin gene promoter polymorphisms and expression levels in Graves' disease and Graves' ophthalmopathy.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 1, doi. 10.1186/1471-2350-13-116

By:

Kun-Hsi Tsai;
Fuu-Jen Tsai;
Hui-Ju Lin;
Hung-Jung Lin;
Yu-Huei Liu;
Wen-Ling Liao;
Lei Wan

Publication type:

Article

Whole-exome sequencing of a pedigree segregating asthma.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 1, doi. 10.1186/1471-2350-13-95

By:

DeWan, Andrew T.;
Egan, Kathryn Brigham;
Hellenbrand, Karen;
Sorrentino, Keli;
Pizzoferrato, Nicole;
Walsh, Kyle M.;
Bracken, Michael B.

Publication type:

Article

Maternal and offspring fasting glucose and type 2 diabetes-associated genetic variants and cognitive function at age 8: a Mendelian randomization study in the Avon Longitudinal Study of Parents and Children.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 1, doi. 10.1186/1471-2350-13-90

By:

Bonilla, Carolina;
Lawlor, Debbie A.;
Ben-Shlomo, Yoav;
Ness, Andrew R.;
Gunnell, David;
Ring, Susan M.;
Smith, George Davey;
Lewis, Sarah J.

Publication type:

Article

A partial MECP2 duplication in a mildly affected adult male: a putative role for the 3' untranslated region in the MECP2 duplication phenotype.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 1, doi. 10.1186/1471-2350-13-71

By:

Hanchard, Neil A.;
Carvalho, Claudia M. B.;
Bader, Patricia;
Thome, Aaron;
Omo-Griffith, Lisa;
del Gaudio, Daniela;
Pehlivan, Davut;
Fang, Ping;
Schaaf, Christian P.;
Ramocki, Melissa B.;
Lupski, James R.;
Cheung, Sau Wai

Publication type:

Article

Transferability and Fine Mapping of genome-wide associated loci for lipids in African Americans.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 1, doi. 10.1186/1471-2350-13-88

By:

Adeyemo, Adebowale;
Bentley, Amy R.;
Meilleur, Katherine G.;
Doumatey, Ayo P.;
Chen, Guanjie;
Zhou, Jie;
Shriner, Daniel;
Huang, Hanxia;
Herbert, Alan;
Gerry, Norman P.;
Christman, Michael F.;
Rotimi, Charles N.

Publication type:

Article

1031-1034delTAAC (Leu125Stop): a novel familial UBE3A mutation causing Angelman syndrome in two siblings showing distinct phenotypes.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 124, doi. 10.1186/1471-2350-13-124

By:

Andreotti De Molfetta, Greice;
Ayres Ferreira, Cristiane;
Onofre Vidal, Daniel;
de Rosso Giuliani, Liane;
Maldonado, Maria Jos‚;
Araujo Silva Jr., Wilson

Publication type:

Article

Genome-wide sequencing for the identification of rearrangements associated with Tourette syndrome and obsessive-compulsive disorder.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 123, doi. 10.1186/1471-2350-13-123

By:

Hooper, Sean D.;
Johansson, Anna C. V.;
Tellgren-Roth, Christian;
Stattin, Eva-Lena;
Dahl, Niklas;
Cavelier, Lucia;
Feuk, Lars

Publication type:

Article

Genotype-phenotype correlation in 22q11.2 deletion syndrome.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 122, doi. 10.1186/1471-2350-13-122

By:

Michaelovsky, Elena;
Frisch, Amos;
Carmel, Miri;
Patya, Miriam;
Zarchi, Omer;
Green, Tamar;
Basel-Vanagaite, Lina;
Weizman, Abraham;
Gothelf, Doron

Publication type:

Article

Phosphodiesterase 8B gene polymorphism in women with recurrent miscarriage: A retrospective case control study.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 121, doi. 10.1186/1471-2350-13-121

By:

Granfors, Michaela;
Karypidis, Helena;
Hosseini, Frida;
Skj”ldebrand-Sparre, Lottie;
Stavreus-Evers, Anneli;
Bremme, Katarina;
Landgren, Britth-Marie;
Sundstr”m-Poromaa, Inger;
Wikstr”m, Anna-Karin;
kerud, Helena

Publication type:

Article

The CAG repeat polymorphism in the Androgen receptor gene modifies the risk for hypospadias in Caucasians.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 109, doi. 10.1186/1471-2350-13-109

By:

Adamovic, Tatjana;
Nordenskj”ld, Agneta

Publication type:

Article

SRY mutation analysis by next generation (deep) sequencing in a cohort of chromosomal Disorders of Sex Development (DSD) patients with a mosaic karyotype.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 108, doi. 10.1186/1471-2350-13-108

By:

Hersmus, Remko;
Stoop, Hans;
Turbitt, Erin;
Oosterhuis, J. Wolter;
Drop, Stenvert L. S.;
Sinclair, Andrew H.;
White, Stefan J.;
Looijenga, Leendert H. J.

Publication type:

Article

Cross-pollination of research findings, although uncommon, may accelerate discovery of human disease genes.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 114, doi. 10.1186/1471-2350-13-114

By:

Duda, Marlena;
Nelson, Tristan;
Wall, Dennis P.

Publication type:

Article

PXR and CAR single nucleotide polymorphisms influence plasma efavirenz levels in South African HIV/AIDS patients.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 112, doi. 10.1186/1471-2350-13-112

By:

Swart, Marelize;
Whitehorn, Heather;
Yuan Ren;
Smith, Peter;
Ramesar, Rajkumar S.;
Dandara, Collet

Publication type:

Article

Novel missense mutation in the RSPO4 gene in congenital hyponychia and evidence for a polymorphic initiation codon (p.M1I).

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 120, doi. 10.1186/1471-2350-13-120

By:

Khan, Tahir Naeem;
Klar, Joakim;
Nawaz, Sadia;
Jameel, Muhammad;
Tariq, Muhammad;
Malik, Naveed Altaf;
Baig, Shahid M;
Dahl, Niklas

Publication type:

Article

Association of SELE genotypes/haplotypes with sE-selectin levels in Taiwanese individuals: interactive effect of MMP9 level.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 115, doi. 10.1186/1471-2350-13-115

By:

Semon Wu;
Lung-An Hsu;
Ming-Sheng Teng;
Jeng-Feng Lin;
Hsien-Hsun Chang;
Yu-Chen Sun;
Hsuan-Pu Chen;
Yu-Lin Ko

Publication type:

Article

A human MYBPC3 mutation appearing about 10 centuries ago results in a hypertrophic cardiomyopathy with delayed onset, moderate evolution but with a risk of sudden death.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 105, doi. 10.1186/1471-2350-13-105

By:

Teirlinck, Carolien H.;
Senni, Fa‹za;
El Malti, Rajae;
Majoor-Krakauer, Danielle;
Fellmann, Florence;
Millat, Gilles;
Andr‚-Fou‰t, Xavier;
Pernot, Fran‡ois;
Stumpf, Micha‰l;
Boutarin, Jean;
Bouvagnet, Patrice

Publication type:

Article

Genetic variant I148M in PNPLA3 is associated with the ultrasonography-determined steatosis degree in a Chinese population.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 113, doi. 10.1186/1471-2350-13-113

By:

Yiling Li;
Chao Xing;
Zhong Tian;
Hung-Chih Ku

Publication type:

Article

Association between XRCC1 polymorphism 399 G->A and glioma among Caucasians: a systematic review and meta-analysis.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 97, doi. 10.1186/1471-2350-13-97

By:

Jacobs, Daniel I.;
Bracken, Michael B.

Publication type:

Article

Adult siblings with homozygous G6PC3 mutations expand our understanding of the severe congenital neutropenia type 4 (SCN4) phenotype.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 111, doi. 10.1186/1471-2350-13-111

By:

Fernandez, Bridget A.;
Green, Jane S.;
Bursey, Ford;
Barrett, Brendan;
MacMillan, Andr‚e;
McColl, Sarah;
Fernandez, Sara;
Rahman, Proton;
Mahoney, Krista;
Pereira, Sergio L.;
Scherer, Stephen W.;
Boycott, Kym M.;
Woods, Michael O.

Publication type:

Article

Association of IL-18 polymorphisms with rheumatoid arthritis and systemic lupus erythematosus in Asian populations: a meta-analysis.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 107, doi. 10.1186/1471-2350-13-107

By:

Shuilian Chen;
Feng Jiang;
Jiangping Ren;
Jiajing Liu;
Wei Meng

Publication type:

Article

APOA5 Q97X Mutation Identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 106, doi. 10.1186/1471-2350-13-106

By:

Dussaillant, Catalina;
Serrano, Valentina;
Maiz, Alberto;
Eyheramendy, Susana;
Cataldo, Luis Rodrigo;
Chavez, Mat¡as;
Smalley, Susan V.;
Fuentes, Marcela;
Rigotti, Attilio;
Rubio, Lorena;
Lagos, Carlos F.;
Martinez, Jos‚ Alfredo;
Santos, Jos‚ Luis

Publication type:

Article

Frank-ter Haar syndrome associated with sagittal craniosynostosis and raised intracranial pressure.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 104, doi. 10.1186/1471-2350-13-104

By:

Bendon, Charlotte L.;
Fenwick, Aim‚e L.;
Hurst, Jane A.;
Nrnberg, Gudrun;
Nrnberg, Peter;
Wall, Steven A.;
Wilkie, Andrew O. M.;
Johnson, David

Publication type:

Article

Association of ALOX5AP gene single nucleotide polymorphisms and cerebral infarction in the Han population of northern China.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 61, doi. 10.1186/1471-2350-13-61

By:

Shuang-yan Zhang;
Mei-ling Xu;
Cui-e Zhang;
Zheng-yi Qu;
Bin-bin Zhang;
Zu-yan Zheng;
Li-ming Zhang

Publication type:

Article

Left ventricular hypertrabeculation/noncompaction with epilepsy, other heart defects, minor facial anomalies and new copy number variants.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 60, doi. 10.1186/1471-2350-13-60

By:

Nagel, Bert;
Gruber-Sedlmayr, Ursula;
Uhrig, Sabine;
St”llberger, Claudia;
Klopocki, Eva;
Finsterer, Finsterer

Publication type:

Article

Association of soluble endothelial protein C receptor plasma levels and PROCR rs867186 with cardiovascular risk factors and cardiovascular events in coronary artery disease patients: The Athero Gene Study.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 103, doi. 10.1186/1471-2350-13-103

By:

Kallel, Choumous;
Cohen, William;
Saut, No‚mie;
Blankenberg, Stefan;
Schnabel, Renate;
Rupprecht, Hans J.;
Bickel, Christoph;
Munzel, Thomas;
Tregouet, David-Alexandre;
Morange, Pierre-Emmanuel

Publication type:

Article

The contribution of FTO and UCP-1 SNPs to extreme obesity, diabetes and cardiovascular risk in Brazilian individuals.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 101, doi. 10.1186/1471-2350-13-101

By:

Ramos, Adauto V.;
Bastos-Rodrigues, Luciana;
Resende, Bruna A.;
Friedman, Eitan;
Campanha-Versiani, Luciana;
Miranda, Debora M.;
Sarquis, Marta;
De Marco, Luiz

Publication type:

Article

Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 94, doi. 10.1186/1471-2350-13-94

By:

Huhn, Stefanie;
Bevier, Melanie;
Rudolph, Anja;
Pardini, Barbara;
Naccarati, Alessio;
Hein, Rebecca;
Hoffmeister, Michael;
Vodickova, Ludmila;
Novotny, Jan;
Brenner, Hermann;
Chang-Claude, Jenny;
Hemminki, Kari;
Vodicka, Pavel;
F”rsti, Asta

Publication type:

Article

MAOA promoter methylation and susceptibility to carotid atherosclerosis: role of familial factors in a monozygotic twin sample.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 100, doi. 10.1186/1471-2350-13-100

By:

Jinying Zhao;
Forsberg, Christopher W.;
Goldberg, Jack;
Smith, Nicholas L.;
Vaccarino, Viola

Publication type:

Article

Subtle mutations in the SMN1 gene in Chinese patients with SMA: p.Arg288Met mutation causing SMN1 transcript exclusion of exon7.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 86, doi. 10.1186/1471-2350-13-86

By:

Qu Yu-jin;
Du Juan;
Li Er-zhen;
Bai Jin-li;
Jin Yu-wei;
Wang Hong;
Song Fang

Publication type:

Article

The identification of a spontaneous 47, XX, +21/46, XY chimeric fetus with male genitalia.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 85, doi. 10.1186/1471-2350-13-85

By:

Kuei-Fang Lee;
Chun-Shuo Hsu;
Pao-Lin Kuo;
Jing-Liang Chen;
Yuan-Hong Jiang;
Liu, Ingrid Y.

Publication type:

Article

High-resolution SNP array analysis of patients with developmental disorder and normal array CGH results.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 84, doi. 10.1186/1471-2350-13-84

By:

Siggberg, Linda;
Sirpa, Ala-Mello;
Tarja, Linnankivi;
Kristiina, Avela;
Ilari, Scheinin;
Kati, Kristiansson;
P„ivi, Lahermo;
Marja, Hietala;
Liisa, Mets„honkala;
Esa, Kuusinen;
Maarit, Laaksonen;
Janna, Saarela;
Sakari, Knuutila

Publication type:

Article

SNP-set analysis replicates acute lung injury genetic risk factors.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 52, doi. 10.1186/1471-2350-13-52

By:

Meyer, Nuala J.;
Daye, Zhongyin John;
Rushefski, Melanie;
Aplenc, Richard;
Lanken, Paul N.;
Shashaty, Michael G. S.;
Christie, Jason D.;
Rui Feng

Publication type:

Article

Cheek swabs, SNP chips, and CNVs: Assessing the quality of copy number variant calls generated with subject-collected mail-in buccal brush DNA samples on a high-density genotyping microarray.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 51, doi. 10.1186/1471-2350-13-51

By:

Erickson, Stephen W.;
MacLeod, Stewart L.;
Hobbs, . Hobbs

Publication type:

Article

A novel multiplex PCR-RFLP method for simultaneous detection of the MTHFR 677 C>T, eNOS +894 G>T and - eNOS -786 T>C variants among Malaysian Malays.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 34, doi. 10.1186/1471-2350-13-34

By:

Keat Wei Loo;
Griffiths, Lyn Robyn;
Siew Hua Gan

Publication type:

Article

Beckwith Wiedemann imprinting defect found in leucocyte but not buccal DNA in a child born small for gestational age.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 99, doi. 10.1186/1471-2350-13-99

By:

Murphy, Rinki;
Mackay, Deborah;
Mitchell, Ed A.

Publication type:

Article

Non-coding RNA ANRIL and the number of plexiform neurofibromas in patients with NF1 microdeletions.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 98, doi. 10.1186/1471-2350-13-98

By:

Muáotter, Tanja;
Kluwe, Lan;
H”gel, Josef;
Nguyen, Rosa;
Cooper, David N.;
Mautner, Victor-Felix;
Kehrer-Sawatzki, Kehrer-Sawatzki

Publication type:

Article

Association of a bitter taste receptor mutation with Balkan Endemic Nephropathy (BEN).

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 96, doi. 10.1186/1471-2350-13-96

By:

Wooding, Stephen P.;
Atanasova, Srebrena;
Gunn, Howard C.;
Staneva, Rada;
Dimova, Invanka;
Toncheva, Toncheva

Publication type:

Article

Identification of a rare 17p13.3 duplication including the BHLHA9 and YWHAE genes in a family with developmental delay and behavioural problems.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 93, doi. 10.1186/1471-2350-13-93

By:

Capra, Valeria;
Mirabelli-Badenier, Marisol;
Stagnaro, Michela;
Rossi, Andrea;
Tassano, Elisa;
Gimelli, Stefania;
Gimelli, Giorgio

Publication type:

Article

T<sup>-786</sup>→C polymorphism of the endothelial nitric oxide synthase gene is associated with insulin resistance in patients with ischemic or non ischemic cardiomyopathy.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 92, doi. 10.1186/1471-2350-13-92

By:

Vecoli, Cecilia;
Grazia Andreassi, Maria;
Liga, Riccardo;
Colombo, Maria;
Coceani, Michele;
Carpeggiani, Clara;
L¨Abbate, Antonio;
Neglia, Danilo

Publication type:

Article

Peripheral PDLIM5 expression in bipolar disorder and the effect of olanzapine administration.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 91, doi. 10.1186/1471-2350-13-91

By:

Aizat Zain, Mohd;
Nusrat Jahan, Suffee;
Reynolds, Gavin P.;
Zuraida Zainal, Nor;
Kanagasundram, Sharmilla;
Mohamed, Mohamed

Publication type:

Article

Expression analyses of the genes harbored by the type 2 diabetes and pediatric BMI associated locus on 10q23.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 89, doi. 10.1186/1471-2350-13-89

By:

Jianhua Zhao;
Deliard, Sandra;
Rahim Aziz, Ali;
Grant, Struan F. A.

Publication type:

Article

Patient accounts of diagnostic testing for familial hypercholesterolaemia: comparing responses to genetic and non-genetic testing methods.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 87, doi. 10.1186/1471-2350-13-87

By:

Hollands, Gareth J.;
Armstrong, David;
Macfarlane, Angela;
Crook, Martin A.;
Marteau, Theresa M.

Publication type:

Article

Quantitative global and gene-specific promoter methylation in relation to biological properties of neuroblastomas.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 83, doi. 10.1186/1471-2350-13-83

By:

Kiss, Nimrod B.;
Kogner, Per;
Inge Johnsen, John;
Martinsson, Tommy;
Larsson, Catharina;
Geli, Geli

Publication type:

Article

PNPLA 3 I148M genetic variant associates with insulin resistance and baseline viral load in HCV genotype 2 but not in genotype 3 infection.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 82, doi. 10.1186/1471-2350-13-82

By:

Rembeck, Rembeck;
Maglio, Cristina;
Lagging, Martin;
Brehm Christensen, Peer;
F„rkkil„, Martti;
Langeland, Nina;
Rauning Buhl, Mads;
Pedersen, Court;
M›rch, Kristine;
Norkrans, Gunnar;
Hellstrand, Kristoffer;
Lindh, Magnus;
Pirazzi, Carlo;
Burza, Maria Antonella;
Romeo, Stefano;
Westin, Johan

Publication type:

Article

A missense founder mutation in VLDLR is associated with Dysequilibrium Syndrome without quadrupedal locomotion.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 80, doi. 10.1186/1471-2350-13-80

By:

Ali, Bassam R.;
Silhavy, Jennifer L.;
Gleeson, Matthew J.;
Gleeson, Joseph G.;
Al-Gazali, Lihadh

Publication type:

Article

UMOD as a susceptibility gene for end-stage renal disease.

Published in:

BMC Medical Genetics, 2012, v. 13, n. 1, p. 78, doi. 10.1186/1471-2350-13-78

By:

Reznichenko, Anna;
B”ger, Carsten A.;
Snieder, Harold;
van den Born, Jacob;
de Borst, Martin H.;
Damman, Jeffrey;
van Dijk, Marcory;
van Goor, Harry;
Hepkema, Bouke G.;
Hillebrands, Jan-Luuk;
Leuvenink, Henri G. D.;
Niesing, Jan;
Bakker, Stephan J. L.;
Seelen, Marc;
Navis, Gerjan

Publication type:

Article