203 related articles for article (PubMed ID: 12552562)
1. The Iranian Human Mutation Gene Bank: a data and sample resource for worldwide collaborative genetics research.
Najmabadi H; Neishabury M; Sahebjam F; Kahrizi K; Shafaghati Y; Nikzat N; Jalalvand M; Aminy F; Hashemi SB; Moghimi B; Noorian AR; Jannati A; Mohammadi M; Javan K;
Hum Mutat; 2003 Feb; 21(2):146-50. PubMed ID: 12552562
[TBL] [Abstract][Full Text] [Related]
2. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Singapore Human Mutation/Polymorphism Database: a country-specific database for mutations and polymorphisms in inherited disorders and candidate gene association studies.
Tan EC; Loh M; Chuon D; Lim YP
Hum Mutat; 2006 Mar; 27(3):232-5. PubMed ID: 16429432
[TBL] [Abstract][Full Text] [Related]
5. Documentation of inherited disorders and mutation frequencies in the different religious communities in Israel in the Israeli National Genetic Database.
Zlotogora J; van Baal S; Patrinos GP
Hum Mutat; 2007 Oct; 28(10):944-9. PubMed ID: 17492749
[TBL] [Abstract][Full Text] [Related]
6. Human gene mutation database-a biomedical information and research resource.
Krawczak M; Ball EV; Fenton I; Stenson PD; Abeysinghe S; Thomas N; Cooper DN
Hum Mutat; 2000; 15(1):45-51. PubMed ID: 10612821
[TBL] [Abstract][Full Text] [Related]
7. The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark.
Jensen HK
Dan Med Bull; 2002 Nov; 49(4):318-45. PubMed ID: 12553167
[TBL] [Abstract][Full Text] [Related]
8. Health-related disparities: influence of environmental factors.
Olden K; White SL
Med Clin North Am; 2005 Jul; 89(4):721-38. PubMed ID: 15925646
[TBL] [Abstract][Full Text] [Related]
9. Hellenic National Mutation database: a prototype database for mutations leading to inherited disorders in the Hellenic population.
Patrinos GP; van Baal S; Petersen MB; Papadakis MN
Hum Mutat; 2005 Apr; 25(4):327-33. PubMed ID: 15776445
[TBL] [Abstract][Full Text] [Related]
10. The human FOXL2 mutation database.
Beysen D; Vandesompele J; Messiaen L; De Paepe A; De Baere E
Hum Mutat; 2004 Sep; 24(3):189-93. PubMed ID: 15300845
[TBL] [Abstract][Full Text] [Related]
11. Contribution of Mendelian disorders to common chronic disease: opportunities for recognition, intervention, and prevention.
Scheuner MT; Yoon PW; Khoury MJ
Am J Med Genet C Semin Med Genet; 2004 Feb; 125C(1):50-65. PubMed ID: 14755434
[TBL] [Abstract][Full Text] [Related]
12. Thailand mutation and variation database (ThaiMUT).
Ruangrit U; Srikummool M; Assawamakin A; Ngamphiw C; Chuechote S; Thaiprasarnsup V; Agavatpanitch G; Pasomsab E; Yenchitsomanus PT; Mahasirimongkol S; Chantratita W; Palittapongarnpim P; Uyyanonvara B; Limwongse C; Tongsima S
Hum Mutat; 2008 Aug; 29(8):E68-75. PubMed ID: 18484585
[TBL] [Abstract][Full Text] [Related]
13. Analysis of the CFTR gene in Iranian cystic fibrosis patients: identification of eight novel mutations.
Alibakhshi R; Kianishirazi R; Cassiman JJ; Zamani M; Cuppens H
J Cyst Fibros; 2008 Mar; 7(2):102-9. PubMed ID: 17662673
[TBL] [Abstract][Full Text] [Related]
14. Arab genetic disease database (AGDDB): a population-specific clinical and mutation database.
Teebi AS; Teebi SA; Porter CJ; Cuticchia AJ
Hum Mutat; 2002 Jun; 19(6):615-21. PubMed ID: 12007218
[TBL] [Abstract][Full Text] [Related]
15. [The origin of informed consent].
Mallardi V
Acta Otorhinolaryngol Ital; 2005 Oct; 25(5):312-27. PubMed ID: 16602332
[TBL] [Abstract][Full Text] [Related]
16. [Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes].
Zhang DL; Ji L; Li YD
Yi Chuan Xue Bao; 2004 May; 31(5):431-43. PubMed ID: 15478601
[TBL] [Abstract][Full Text] [Related]
17. Iranian Breast Cancer Bio-Bank: the activity and challenging issues.
Majidzadeh-A K; Kaviani A; Esmaeili R; Farahmand L; Shojamoradi MH; Zare AA; Eini L; Abbasvandi F; Olfatbakhsh A; Moazen H
Cell Tissue Bank; 2013 Mar; 14(1):11-20. PubMed ID: 22318652
[TBL] [Abstract][Full Text] [Related]
18. [Development of antituberculous drugs: current status and future prospects].
Tomioka H; Namba K
Kekkaku; 2006 Dec; 81(12):753-74. PubMed ID: 17240921
[TBL] [Abstract][Full Text] [Related]
19. A structured simple form for ordering genetic tests is needed to ensure coupling of clinical detail (phenotype) with DNA variants (genotype) to ensure utility in publication and databases.
Cotton RG; Auerbach AD; Brown AF; Carrera P; Christodoulou J; Claustres M; Compton J; Cox DW; De Baere E; den Dunnen JT; Greenblatt M; Fujiwara M; Hilbert P; Jani A; Lehvaslaiho H; Nebert DW; Verma I; Vihinen M; ;
Hum Mutat; 2007 Oct; 28(10):931-2. PubMed ID: 17726697
[TBL] [Abstract][Full Text] [Related]
20. A community genetics perspective on consanguineous marriage.
Bittles AH
Community Genet; 2008; 11(6):324-30. PubMed ID: 18690000
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]