BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

119 related articles for article (PubMed ID: 2004784)

  • 1. Fanconi anemia: evidence for linkage heterogeneity on chromosome 20q.
    Mann WR; Venkatraj VS; Allen RG; Liu Q; Olsen DA; Adler-Brecher B; Mao JI; Weiffenbach B; Sherman SL; Auerbach AD
    Genomics; 1991 Feb; 9(2):329-37. PubMed ID: 2004784
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A locus for Fanconi anemia on 16q determined by homozygosity mapping.
    Gschwend M; Levran O; Kruglyak L; Ranade K; Verlander PC; Shen S; Faure S; Weissenbach J; Altay C; Lander ES; Auerbach AD; Botstein D
    Am J Hum Genet; 1996 Aug; 59(2):377-84. PubMed ID: 8755924
    [TBL] [Abstract][Full Text] [Related]  

  • 3. D20S19, linked to low voltage EEG, benign neonatal convulsions, and Fanconi anaemia, maps to a region of enhanced recombination and is localized between CpG islands.
    Steinlein O; Fischer C; Keil R; Smigrodzki R; Vogel F
    Hum Mol Genet; 1992 Aug; 1(5):325-9. PubMed ID: 1303209
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Localisation of the Fanconi anaemia complementation group A gene to chromosome 16q24.3.
    Pronk JC; Gibson RA; Savoia A; Wijker M; Morgan NV; Melchionda S; Ford D; Temtamy S; Ortega JJ; Jansen S
    Nat Genet; 1995 Nov; 11(3):338-40. PubMed ID: 7581462
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Localization of a gene for the human low-voltage EEG on 20q and genetic heterogeneity.
    Steinlein O; Anokhin A; Yping M; Schalt E; Vogel F
    Genomics; 1992 Jan; 12(1):69-73. PubMed ID: 1346390
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Confirmation of linkage of benign familial neonatal convulsions to D20S19 and D20S20.
    Malafosse A; Leboyer M; Dulac O; Navelet Y; Plouin P; Beck C; Laklou H; Mouchnino G; Grandscene P; Vallee L
    Hum Genet; 1992 Apr; 89(1):54-8. PubMed ID: 1577466
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Linkage analysis of Fanconi anaemia in Italy and mapping of the complementation group A gene.
    Savoia A; Piemontese MR; Savino M; Zatterale A; Pronk J; Arwert F; Joenje H; Ramenghi U; Dagna-Bricarelli F; Dallapiccola B; Zelante L
    Hum Genet; 1997 Jan; 99(1):93-7. PubMed ID: 9003502
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evidence for linkage of familial Diamond-Blackfan anemia to chromosome 8p23.3-p22 and for non-19q non-8p disease.
    Gazda H; Lipton JM; Willig TN; Ball S; Niemeyer CM; Tchernia G; Mohandas N; Daly MJ; Ploszynska A; Orfali KA; Vlachos A; Glader BE; Rokicka-Milewska R; Ohara A; Baker D; Pospisilova D; Webber A; Viskochil DH; Nathan DG; Beggs AH; Sieff CA
    Blood; 2001 Apr; 97(7):2145-50. PubMed ID: 11264183
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Benign familial neonatal convulsions: confirmation of genetic heterogeneity and further evidence for a second locus on chromosome 8q.
    Steinlein O; Schuster V; Fischer C; Häussler M
    Hum Genet; 1995 Apr; 95(4):411-5. PubMed ID: 7705837
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic mapping of the FACC gene and linkage analysis in Fanconi anaemia families.
    Gibson RA; Ford D; Jansen S; Savoia A; Havenga C; Milner RD; de Ravel TJ; Cohn RJ; Ball SE; Roberts I
    J Med Genet; 1994 Nov; 31(11):868-71. PubMed ID: 7853372
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Fanconi anemia: a model for genetic causes of abnormal brain development.
    Pavlakis SG; Frissora CL; Giampietro PF; Davis JG; Gould RJ; Adler-Brecher B; Auerbach AD
    Dev Med Child Neurol; 1992 Dec; 34(12):1081-4. PubMed ID: 1451937
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A microsatellite polymorphism associated with the PLC1 (phospholipase C) locus: identification, mapping, and linkage to the MODY locus on chromosome 20.
    Rothschild CB; Akots G; Fajans SS; Bowden DW
    Genomics; 1992 Jul; 13(3):560-4. PubMed ID: 1639386
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Evidence for linkage of the gene causing familial Mediterranean fever to chromosome 17q in non-Ashkenazi Jewish families: second locus or type I error?
    Aksentijevich I; Gruberg L; Pras E; Balow JE; Kovo M; Gazit E; Dean M; Pras M; Kastner DL
    Hum Genet; 1993 Jul; 91(6):527-34. PubMed ID: 8340105
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The Fanconi anemia group E gene, FANCE, maps to chromosome 6p.
    Waisfisz Q; Saar K; Morgan NV; Altay C; Leegwater PA; de Winter JP; Komatsu K; Evans GR; Wegner RD; Reis A; Joenje H; Arwert F; Mathew CG; Pronk JC; Digweed M
    Am J Hum Genet; 1999 May; 64(5):1400-5. PubMed ID: 10205272
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Restless legs syndrome: confirmation of linkage to chromosome 12q, genetic heterogeneity, and evidence of complexity.
    Desautels A; Turecki G; Montplaisir J; Xiong L; Walters AS; Ehrenberg BL; Brisebois K; Desautels AK; Gingras Y; Johnson WG; Lugaresi E; Coccagna G; Picchietti DL; Lazzarini A; Rouleau GA
    Arch Neurol; 2005 Apr; 62(4):591-6. PubMed ID: 15824258
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14.
    Bejaoui K; Hirabayashi K; Hentati F; Haines JL; Ben Hamida C; Belal S; Miller RG; McKenna-Yasek D; Weissenbach J; Rowland LP
    Neurology; 1995 Apr; 45(4):768-72. PubMed ID: 7723968
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic and physical mapping of the locus for autosomal dominant renal Fanconi syndrome, on chromosome 15q15.3.
    Lichter-Konecki U; Broman KW; Blau EB; Konecki DS
    Am J Hum Genet; 2001 Jan; 68(1):264-8. PubMed ID: 11090339
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic linkage study of familial Mediterranean fever (FMF) to 16p13.3 and evidence for genetic heterogeneity in the Turkish population.
    Akarsu AN; Saatci U; Ozen S; Bakkaloglu A; Besbas N; Sarfarazi M
    J Med Genet; 1997 Jul; 34(7):573-8. PubMed ID: 9222966
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Localisation of a Fanconi anaemia gene to chromosome 9p.
    Saar K; Schindler D; Wegner RD; Reis A; Wienker TF; Hoehn H; Joenje H; Sperling K; Digweed M
    Eur J Hum Genet; 1998; 6(5):501-8. PubMed ID: 9801875
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Linkage mapping of new X-linked juvenile retinoschisis kindreds using microsatellite markers.
    Shastry BS; Hejtmancik FJ; Margherio RT; Trese MT
    Biochem Biophys Res Commun; 1996 Mar; 220(3):824-7. PubMed ID: 8607849
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.