Luis Carvajal-Carmona

Luis Carvajal-Carmona

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Luis Carvajal-Carmona

Luis Carvajal-Carmona

Publications by authors named "Luis Carvajal-Carmona"

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BRAF and TERT mutations in papillary thyroid cancer patients of Latino ancestry.

Endocr Connect 2019 Aug 1. Epub 2019 Aug 1.

L Carvajal-Carmona, Genome Center, Department of Biochemistry and molecular medicine, University of California, Davis, United States.

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http://dx.doi.org/10.1530/EC-19-0376DOI Listing
August 2019

Racial/ethnic differences in survival among gastric cancer patients in california.

Cancer Causes Control 2019 Jul 17;30(7):687-696. Epub 2019 May 17.

Public Health Institute, Cancer Registry of Greater California, 1825 Bell St, Ste 102, Sacramento, CA, USA.

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http://dx.doi.org/10.1007/s10552-019-01184-0DOI Listing
July 2019

Identification of novel common breast cancer risk variants at the 6q25 locus among Latinas.

Breast Cancer Res 2019 01 14;21(1). Epub 2019 Jan 14.

Division of General Internal Medicine, Department of Medicine, Institute of Human Genetics, Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, Box 0320, San Francisco, CA, 94143, USA.

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https://breast-cancer-research.biomedcentral.com/articles/10
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http://dx.doi.org/10.1186/s13058-018-1085-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332913PMC
January 2019

Resolving gastric cancer aetiology: an update in genetic predisposition.

Lancet Gastroenterol Hepatol 2018 12;3(12):874-883

Genome Center, School of Medicine, University of California at Davis, Davis, CA, USA; Population Sciences and Cancer Health Disparities Program, UC Davis Comprehensive Cancer Center, School of Medicine, University of California at Davis, Davis, CA, USA; Department of Biochemistry and Molecular Medicine, School of Medicine, University of California at Davis, Davis, CA, USA. Electronic address:

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http://dx.doi.org/10.1016/S2468-1253(18)30237-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6500447PMC
December 2018

Moving the needle on colorectal cancer genetics: it takes more than two to TANGO.

Br J Cancer 2018 10 4;119(8):913-914. Epub 2018 Oct 4.

Genome Center, University of California, Davis, CA, USA.

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http://dx.doi.org/10.1038/s41416-018-0219-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6203804PMC
October 2018

Native American gene continuity to the modern admixed population from the Colombian Andes: Implication for biomedical, population and forensic studies.

Forensic Sci Int Genet 2018 09 7;36:e1-e7. Epub 2018 Jun 7.

Grupo de Citogenética, Filogenia y Evolución de Poblaciones, Facultad de Ciencias y Facultad de Ciencias de la Salud, Universidad del Tolima, Ibagué, Colombia; Fundación de Genética y Genómica, Medellin, Colombia; Corporación Universitaria Remington, Medellin, Colombia; Genome Center and Department of Biochemistry and Molecular Medicine, School of Medicine, University of California, Davis, GBSF, 451 Health Science Drive Davis, CA, 95616-8816, USA. Electronic address:

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http://dx.doi.org/10.1016/j.fsigen.2018.06.006DOI Listing
September 2018

PALB2 as a familial gastric cancer gene: is the wait over?

Lancet Gastroenterol Hepatol 2018 07 27;3(7):451-452. Epub 2018 Apr 27.

Genome Center and Department of Biochemistry and Molecular Medicine, University of California, Davis, CA 95616, USA. Electronic address:

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http://dx.doi.org/10.1016/S2468-1253(18)30120-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6474236PMC
July 2018

Methods for Scarless, Selection-Free Generation of Human Cells and Allele-Specific Functional Analysis of Disease-Associated SNPs and Variants of Uncertain Significance.

Sci Rep 2017 11 8;7(1):15044. Epub 2017 Nov 8.

Genome Center and Department of Biochemistry and Molecular Medicine, University of California, Davis, Davis, CA, 95616, USA.

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http://dx.doi.org/10.1038/s41598-017-15407-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5678142PMC
November 2017

and founder mutations account for 78% of germline carriers among hereditary breast cancer families in Chile.

Oncotarget 2017 Sep 29;8(43):74233-74243. Epub 2017 Jun 29.

Department of Cell and Molecular Biology, Faculty of Biological Sciences, Pontificia Universidad Católica de Chile, Santiago, Chile.

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http://dx.doi.org/10.18632/oncotarget.18815DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5650336PMC
September 2017

Clinical manifestations of colorectal cancer patients from a large multicenter study in Colombia.

Medicine (Baltimore) 2016 Oct;95(40):e4883

aGenome Center and Department of Biochemistry and Molecular Medicine, School of Medicine, University of California, Davis, CA bGrupo de Investigación Citogenética, Filogenia y Evolución de Poblaciones, Facultades de Ciencias y de Ciencias de Salud, Universidad del Tolima, Ibagué, Colombia cInstituto Nacional de Cancerología, Bogotá, DC, Colombia dHospital Pablo Tobón Uribe, Medellín, Colombia eHospital Federico Lleras Acosta, Ibagué, Colombia fClinica Las Américas, Medellín, Colombia gHospital Hernando Moncaleano Perdomo, Neiva, Colombia hUniversidad Surcolombiana, Neiva, Colombia iPatologos Asociados Tolima, Ibagué, Colombia jWellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK kFundación de Genética y Genómica, Medellín, Colombia.

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http://dx.doi.org/10.1097/MD.0000000000004883DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5059046PMC
October 2016

RE: HABP2 G534E Mutation in Familial Nonmedullary Thyroid Cancer.

J Natl Cancer Inst 2016 08 6;108(8). Epub 2016 May 6.

Genome Center and Department of Biochemistry and Molecular Medicine, School of Medicine, University of California, Davis, Davis, CA (LGCC, RS); Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK (IT).

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http://dx.doi.org/10.1093/jnci/djw108DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5017950PMC
August 2016

Clinical features of Hispanic thyroid cancer cases and the role of known genetic variants on disease risk.

Medicine (Baltimore) 2016 Aug;95(32):e4148

aGrupo de Citogenética, Filogenia y Evolución de Poblaciones, Facultad de Ciencias y Facultad de Ciencias de la Salud, Universidad del Tolima, Ibagué, Colombia bGenome Center and Department of Biochemistry and Molecular Medicine, School of Medicine, University of California, Davis, CA cHospital Pablo Tobón Uribe, Medellín dHospital Federico Lleras Acosta, Ibagué eHospital Hernando Moncaleano Perdomo, Neiva fFundación de Genética y Genómica, Medellín, Colombia.

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http://dx.doi.org/10.1097/MD.0000000000004148DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4985291PMC
August 2016

The Hunting of the Snark: Whither Genome-Wide Association Studies for Colorectal Cancer?

Gastroenterology 2016 06 29;150(7):1528-1530. Epub 2016 Apr 29.

Oxford Centre for Cancer Gene Research, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.

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http://dx.doi.org/10.1053/j.gastro.2016.04.021DOI Listing
June 2016

The HABP2 G534E polymorphism does not increase nonmedullary thyroid cancer risk in Hispanics.

Endocr Connect 2016 May 20;5(3):123-7. Epub 2016 Apr 20.

Grupo de CitogenéticaFilogenia y Evolución de Poblaciones, Facultad de Ciencias y Facultad de Ciencias de la Salud, Universidad del Tolima, Ibagué, Colombia Genome Center and Department of Biochemistry and Molecular MedicineSchool of Medicine, University of California, Davis, California, USA Fundación de Genética y GenómicaMedellín, Colombia

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http://dx.doi.org/10.1530/EC-16-0017DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5002962PMC
May 2016

The HABP2 G534E variant is an unlikely cause of familial non-medullary thyroid cancer.

J Clin Endocrinol Metab 2016 03 21;10(3):1098-1103. Epub 2015 Dec 21.

Genome Center and Department of Biochemistry and Molecular Medicine, School of Medicine, University of California, Davis, USA.

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http://dx.doi.org/10.1210/jc.2015-3928DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4803181PMC
March 2016

CYP19A1 fine-mapping and Mendelian randomization: estradiol is causal for endometrial cancer.

Endocr Relat Cancer 2016 Feb 16;23(2):77-91. Epub 2015 Nov 16.

Department of Public Health and Primary CareCentre for Cancer Genetic Epidemiology, University of Cambridge, Strangeways Research Laboratory, Worts Causeway, Cambridge, Cambridge CB1 8RN, UKDepartment of Genetics and Computational BiologyQIMR Berghofer Medical Research Institute, Brisbane, Queensland, 4006, AustraliaWellcome Trust Centre for Human GeneticsUniversity of Oxford, Oxford OX3 7BN, UKAcademic Department of BiochemistryRoyal Marsden Hospital, London SW3 6JJ, UKDepartment of Clinical GeneticsSt George's Hospital Medical School, London SW17 0RE, UKDepartment of OncologyCentre for Cancer Genetic Epidemiology, University of Cambridge, Cambridge CB1 8RN, UKDepartment of Medical Epidemiology and BiostatisticsKarolinska Institutet, Stockholm SE-171 77, SwedenDepartment of MedicineDivision of Hematology/Oncology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California 90095, USADepartment of Gynecology and ObstetricsUniversity Hospital Erlangen, Friedrich-Alexander-University Erlangen-Nuremberg, Erlangen 91054, GermanyInstitute of Human GeneticsUniversity Hospital Erlangen, Friedrich-Alexander-University Erlangen-Nuremberg, Erlangen 91054, GermanyGynaecology Research UnitHannover Medical School, Hannover 30625, GermanyClinics of Gynaecology and ObstetricsHannover Medical School, Hannover 30625, GermanyDepartment of GynaecologyJena University Hospital - Friedrich Schiller University, Jena 07743, GermanyVesalius Research CenterLeuven 3000, BelgiumLaboratory for Translational GeneticsDepartment of Oncology, University Hospitals Leuven, Leuven 3000, BelgiumDepartment of Obstetrics and GynecologyDivision of Gynecologic Oncology, University Hospitals, KU Leuven - University of Leuven, Leuven 3000, BelgiumDepartment of Health Sciences ResearchMayo Clinic, Rochester, Minnesota 55905, USADepartment of BiostatisticsUniversity of Kansas Medical Center, Kansas City, Kansas 66160, USADepartment of Obstetrics and GynecologyDivision of G

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http://dx.doi.org/10.1530/ERC-15-0386DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4697192PMC
February 2016

Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.

Authors:
Timothy H T Cheng Deborah Thompson Jodie Painter Tracy O'Mara Maggie Gorman Lynn Martin Claire Palles Angela Jones Daniel D Buchanan Aung Ko Win John Hopper Mark Jenkins Noralane M Lindor Polly A Newcomb Steve Gallinger David Conti Fred Schumacher Graham Casey Graham G Giles Paul Pharoah Julian Peto Angela Cox Anthony Swerdlow Fergus Couch Julie M Cunningham Ellen L Goode Stacey J Winham Diether Lambrechts Peter Fasching Barbara Burwinkel Hermann Brenner Hiltrud Brauch Jenny Chang-Claude Helga B Salvesen Vessela Kristensen Hatef Darabi Jingmei Li Tao Liu Annika Lindblom Per Hall Magdalena Echeverry de Polanco Monica Sans Angel Carracedo Sergi Castellvi-Bel Augusto Rojas-Martinez Samuel Aguiar Jnr Manuel R Teixeira Alison M Dunning Joe Dennis Geoffrey Otton Tony Proietto Elizabeth Holliday John Attia Katie Ashton Rodney J Scott Mark McEvoy Sean C Dowdy Brooke L Fridley Henrica M J Werner Jone Trovik Tormund S Njolstad Emma Tham Miriam Mints Ingo Runnebaum Peter Hillemanns Thilo Dörk Frederic Amant Stefanie Schrauwen Alexander Hein Matthias W Beckmann Arif Ekici Kamila Czene Alfons Meindl Manjeet K Bolla Kyriaki Michailidou Jonathan P Tyrer Qin Wang Shahana Ahmed Catherine S Healey Mitul Shah Daniela Annibali Jeroen Depreeuw Nada A Al-Tassan Rebecca Harris Brian F Meyer Nicola Whiffin Fay J Hosking Ben Kinnersley Susan M Farrington Maria Timofeeva Albert Tenesa Harry Campbell Robert W Haile Shirley Hodgson Luis Carvajal-Carmona Jeremy P Cheadle Douglas Easton Malcolm Dunlop Richard Houlston Amanda Spurdle Ian Tomlinson

Sci Rep 2015 12 1;5:17369. Epub 2015 Dec 1.

Molecular and Population Genetics Laboratory, Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford OX3 7BN, UK.

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http://dx.doi.org/10.1038/srep17369DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4664893PMC
December 2015

Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk.

Authors:
Jodie N Painter Tracy A O'Mara Jyotsna Batra Timothy Cheng Felicity A Lose Joe Dennis Kyriaki Michailidou Jonathan P Tyrer Shahana Ahmed Kaltin Ferguson Catherine S Healey Susanne Kaufmann Kristine M Hillman Carina Walpole Leire Moya Pamela Pollock Angela Jones Kimberley Howarth Lynn Martin Maggie Gorman Shirley Hodgson Ma Magdalena Echeverry De Polanco Monica Sans Angel Carracedo Sergi Castellvi-Bel Augusto Rojas-Martinez Erika Santos Manuel R Teixeira Luis Carvajal-Carmona Xiao-Ou Shu Jirong Long Wei Zheng Yong-Bing Xiang Grant W Montgomery Penelope M Webb Rodney J Scott Mark McEvoy John Attia Elizabeth Holliday Nicholas G Martin Dale R Nyholt Anjali K Henders Peter A Fasching Alexander Hein Matthias W Beckmann Stefan P Renner Thilo Dörk Peter Hillemanns Matthias Dürst Ingo Runnebaum Diether Lambrechts Lieve Coenegrachts Stefanie Schrauwen Frederic Amant Boris Winterhoff Sean C Dowdy Ellen L Goode Attila Teoman Helga B Salvesen Jone Trovik Tormund S Njolstad Henrica M J Werner Katie Ashton Tony Proietto Geoffrey Otton Gerasimos Tzortzatos Miriam Mints Emma Tham Per Hall Kamila Czene Jianjun Liu Jingmei Li John L Hopper Melissa C Southey Arif B Ekici Matthias Ruebner Nicola Johnson Julian Peto Barbara Burwinkel Frederik Marme Hermann Brenner Aida K Dieffenbach Alfons Meindl Hiltrud Brauch Annika Lindblom Jeroen Depreeuw Matthieu Moisse Jenny Chang-Claude Anja Rudolph Fergus J Couch Janet E Olson Graham G Giles Fiona Bruinsma Julie M Cunningham Brooke L Fridley Anne-Lise Børresen-Dale Vessela N Kristensen Angela Cox Anthony J Swerdlow Nicholas Orr Manjeet K Bolla Qin Wang Rachel Palmieri Weber Zhihua Chen Mitul Shah Juliet D French Paul D P Pharoah Alison M Dunning Ian Tomlinson Douglas F Easton Stacey L Edwards Deborah J Thompson Amanda B Spurdle

Hum Mol Genet 2015 Mar 6;24(5):1478-92. Epub 2014 Nov 6.

QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia,

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http://dx.doi.org/10.1093/hmg/ddu552DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4321445PMC
March 2015

Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk.

Hum Genet 2015 Feb 9;134(2):231-45. Epub 2014 Dec 9.

Genome Center and Department of Biochemistry and Molecular Medicine, School of Medicine, University of California, Davis, CA, 95616, USA,

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http://dx.doi.org/10.1007/s00439-014-1515-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4291520PMC
February 2015

Germline variants and advanced colorectal adenomas: adenoma prevention with celecoxib trial genome-wide association study.

Clin Cancer Res 2013 Dec 1;19(23):6430-7. Epub 2013 Oct 1.

Authors' Affiliations: Department of Surgery, Division of Surgical Oncology, Center for Genomic Medicine, Channing Laboratory, Brigham and Women's Hospital, Boston, Massachusetts; Genome Center and Department of Biochemistry and Molecular Medicine, University of California, Davis, California; Department of Epidemiology and Statistics, Memorial Sloan-Kettering Cancer Center, New York; RIKEN Center for Genomic Medicine, Tokyo, Japan; Colon Cancer Genetics Group, Institute of Genetics and Molecular Medicine, University of Edinburgh and MRC Human Genetics Unit, Edinburgh; Section of Cancer Genetics, Institute of Cancer Research, Sutton, United Kingdom; Ludwig Colon Cancer Initiative Laboratory, Ludwig Institute for Cancer Research, Royal Melbourne Hospital, Parkville; Genetic and Molecular Epidemiology Laboratories, and Familial Cancer laboratory, Queensland Institute of Medical Research, Brisbane; Centre for Eye Research Australia, University of Melbourne, Royal Victorian Eye and Ear Hospital, East Melbourne, Australia; and Department of Medicine, University of Chicago, Chicago, Illinois.

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http://dx.doi.org/10.1158/1078-0432.CCR-13-0550DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4037290PMC
December 2013

Novel MLH1 duplication identified in Colombian families with Lynch syndrome.

Genet Med 2011 Feb;13(2):155-60

Gastroenterology Department, Institut de Malalties Digestives i Metabòliques, Hospital Clínic, CIBEREHD, IDIBAPS, University of Barcelona, Barcelona, Catalonia, Spain.

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http://dx.doi.org/10.1097/GIM.0b013e318202e10bDOI Listing
February 2011

Genetic dissection of intermediate phenotypes as a way to discover novel cancer susceptibility alleles.

Curr Opin Genet Dev 2010 Jun 24;20(3):308-14. Epub 2010 Apr 24.

Molecular and Population Genetics, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.

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http://dx.doi.org/10.1016/j.gde.2010.03.013DOI Listing
June 2010

Challenges in the identification and use of rare disease-associated predisposition variants.

Curr Opin Genet Dev 2010 Jun;20(3):277-81

Molecular and Population Genetics, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.

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June 2010

Comprehensive assessment of variation at the transforming growth factor beta type 1 receptor locus and colorectal cancer predisposition.

Proc Natl Acad Sci U S A 2010 Apr 5;107(17):7858-62. Epub 2010 Apr 5.

Molecular and Population Genetics Laboratory, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, United Kingdom.

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http://dx.doi.org/10.1073/pnas.1002816107DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2867909PMC
April 2010

Colorectal cancer risk is not associated with increased levels of homozygosity in a population from the United Kingdom.

Cancer Res 2009 Sep 1;69(18):7422-9. Epub 2009 Sep 1.

The Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.

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http://dx.doi.org/10.1158/0008-5472.CAN-09-0659DOI Listing
September 2009

Common variation at the adiponectin locus is not associated with colorectal cancer risk in the UK.

Hum Mol Genet 2009 May 5;18(10):1889-92. Epub 2009 Mar 5.

Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.

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http://dx.doi.org/10.1093/hmg/ddp109DOI Listing
May 2009

A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3.

Nat Genet 2008 May 30;40(5):623-30. Epub 2008 Mar 30.

Molecular and Population Genetics Laboratory, London Research Institute, Cancer Research UK, London WC2A 3PX, UK.

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http://dx.doi.org/10.1038/ng.111DOI Listing
May 2008

A family with juvenile polyposis linked to the BMPR1A locus: cryptic mutation or closely linked gene?

J Gastroenterol Hepatol 2007 Dec 15;22(12):2292-7. Epub 2007 Jun 15.

Department of Colorectal Medicine and Genetics, The Royal Melbourne Hospital, Melbourne, Victoria, Australia.

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http://dx.doi.org/10.1111/j.1440-1746.2007.04989.xDOI Listing
December 2007

Adult leydig cell tumors of the testis caused by germline fumarate hydratase mutations.

J Clin Endocrinol Metab 2006 Aug 6;91(8):3071-5. Epub 2006 Jun 6.

Laboratory of Molecular and Population Genetics, London Research Institute, Cancer Research UK, London WC2A 3PX, United Kingdom.

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http://dx.doi.org/10.1210/jc.2006-0183DOI Listing
August 2006

EPHB2 germline variants in patients with colorectal cancer or hyperplastic polyposis.

BMC Cancer 2006 Jun 1;6:145. Epub 2006 Jun 1.

Department of Medical Genetics, Molecular and Cancer Biology Research Program, P,O, BOX 63, 00014 University of Helsinki, Finland.

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http://dx.doi.org/10.1186/1471-2407-6-145DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1513590PMC
June 2006

Abundant mtDNA diversity and ancestral admixture in Colombian criollo cattle (Bos taurus).

Genetics 2003 Nov;165(3):1457-63

Galton Laboratory, Department of Biology, University College, London NW1 2HE, United Kingdom.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1462844PMC
November 2003

Genetic demography of Antioquia (Colombia) and the Central Valley of Costa Rica.

Hum Genet 2003 May 25;112(5-6):534-41. Epub 2003 Feb 25.

The Galton Laboratory, Department of Biology (Wolfson House), University College London, UK.

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http://dx.doi.org/10.1007/s00439-002-0899-8DOI Listing
May 2003