These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

159 related articles for article (PubMed ID: 9915956)

  • 21. Sequence analysis of the granulysin and granzyme B genes in familial hemophagocytic lymphohistiocytosis.
    Ericson KG; Fadeel B; Andersson M; Gudmundsson GH; Gürgey A; Yalman N; Janka G; Nordenskjöld M; Henter JI
    Hum Genet; 2003 Jan; 112(1):98-9. PubMed ID: 12483306
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A novel locus for idiopathic generalized epilepsy in French-Canadian families maps to 10p11.
    Kinirons P; Verlaan DJ; Dubé MP; Poirier J; Deacon C; Lortie A; Clément JF; Desbiens R; Carmant L; Cieuta-Walti C; Shevell M; Rouleau GA; Cossette P
    Am J Med Genet A; 2008 Mar; 146A(5):578-84. PubMed ID: 18241056
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Familial hemophagocytic lymphohistiocytosis: an autopsy study.
    Kakkar N; Vasishta RK; Banerjee AK; Marwaha RK; Thapa BR
    Pediatr Pathol Mol Med; 2003; 22(3):229-42. PubMed ID: 12746174
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Familial hyperaldosteronism type II is linked to the chromosome 7p22 region but also shows predicted heterogeneity.
    So A; Duffy DL; Gordon RD; Jeske YW; Lin-Su K; New MI; Stowasser M
    J Hypertens; 2005 Aug; 23(8):1477-84. PubMed ID: 16003173
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Linkage and LOH studies in 19 cylindromatosis families show no evidence of genetic heterogeneity and refine the CYLD locus on chromosome 16q12-q13.
    Takahashi M; Rapley E; Biggs PJ; Lakhani SR; Cooke D; Hansen J; Blair E; Hofmann B; Siebert R; Turner G; Evans DG; Schrander-Stumpel C; Beemer FA; van Vloten WA; Breuning MH; van den Ouweland A; Halley D; Delpech B; Cleveland M; Leigh I; Chapman P; Burn J; Hohl D; Görög JP; Seal S; Mangion J
    Hum Genet; 2000 Jan; 106(1):58-65. PubMed ID: 10982183
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A gene locus responsible for the familial hair shaft abnormality pili annulati maps to chromosome 12q24.32-24.33.
    Giehl KA; Eckstein GN; Benet-Pagès A; Tosti A; de Berker DA; Meitinger T; Müller-Myhsok B; Strom TM
    J Invest Dermatol; 2004 Dec; 123(6):1073-7. PubMed ID: 15610517
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A new locus for autosomal dominant "pure" hereditary spastic paraplegia mapping to chromosome 12q13, and evidence for further genetic heterogeneity.
    Reid E; Dearlove AM; Rhodes M; Rubinsztein DC
    Am J Hum Genet; 1999 Sep; 65(3):757-63. PubMed ID: 10441583
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Familial juvenile hyperuricemic nephropathy: localization of the gene on chromosome 16p11.2-and evidence for genetic heterogeneity.
    Stibůrková B; Majewski J; Sebesta I; Zhang W; Ott J; Kmoch S
    Am J Hum Genet; 2000 Jun; 66(6):1989-94. PubMed ID: 10780922
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Mapping of the familial infantile myasthenia (congenital myasthenic syndrome type Ia) gene to chromosome 17p with evidence of genetic homogeneity.
    Christodoulou K; Tsingis M; Deymeer F; Serdaroglu P; Ozdemir C; Al-Shehab A; Bairactaris C; Mavromatis I; Mylonas I; Evoli A; Kyriallis K; Middleton LT
    Hum Mol Genet; 1997 Apr; 6(4):635-40. PubMed ID: 9097970
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Hereditary geniospasm: linkage to chromosome 9q13-q21 and evidence for genetic heterogeneity.
    Jarman PR; Wood NW; Davis MT; Davis PV; Bhatia KP; Marsden CD; Davis MB
    Am J Hum Genet; 1997 Oct; 61(4):928-33. PubMed ID: 9382105
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Familial typical migraine: linkage to chromosome 19p13 and evidence for genetic heterogeneity.
    Nyholt DR; Lea RA; Goadsby PJ; Brimage PJ; Griffiths LR
    Neurology; 1998 May; 50(5):1428-32. PubMed ID: 9596000
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia.
    Ashley-Koch A; Bonner ER; Gaskell PC; West SG; Tim R; Wolpert CM; Jones R; Farrell CD; Nance M; Svenson IK; Marchuk DA; Boustany RM; Vance JM; Scott WK; Pericak-Vance MA
    Neurogenetics; 2001 Mar; 3(2):91-7. PubMed ID: 11354831
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A locus for autosomal dominant reflex epilepsy precipitated by hot water maps at chromosome 10q21.3-q22.3.
    Ratnapriya R; Satishchandra P; Kumar SD; Gadre G; Reddy R; Anand A
    Hum Genet; 2009 Jun; 125(5-6):541-9. PubMed ID: 19266219
    [TBL] [Abstract][Full Text] [Related]  

  • 35. EBV-elicited familial hemophagocytic lymphohistiocytosis.
    Cho HS; Park YN; Lyu CJ; Park SM; Oh SH; Yang CH; Yang WI; Kim KY
    Yonsei Med J; 1997 Aug; 38(4):245-8. PubMed ID: 9339134
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Confirmation of genetic heterogeneity in familial psoriasis.
    Matthews D; Fry L; Powles A; Weissenbach J; Williamson R
    J Med Genet; 1995 Jul; 32(7):546-8. PubMed ID: 7562968
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Linkage analysis of candidate regions in Swedish nonsyndromic cleft lip with or without cleft palate families.
    Wong FK; Hagberg C; Karsten A; Larson O; Gustavsson M; Huggare J; Larsson C; Teh BT; Linder-Aronson S
    Cleft Palate Craniofac J; 2000 Jul; 37(4):357-62. PubMed ID: 10912714
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Evidence for a nonallelic heterogeneity of epidermodysplasia verruciformis with two susceptibility loci mapped to chromosome regions 2p21-p24 and 17q25.
    Ramoz N; Taïeb A; Rueda LA; Montoya LS; Bouadjar B; Favre M; Orth G
    J Invest Dermatol; 2000 Jun; 114(6):1148-53. PubMed ID: 10844558
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Hereditary lymphedema: evidence for linkage and genetic heterogeneity.
    Ferrell RE; Levinson KL; Esman JH; Kimak MA; Lawrence EC; Barmada MM; Finegold DN
    Hum Mol Genet; 1998 Dec; 7(13):2073-8. PubMed ID: 9817924
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Evidence of genetic heterogeneity in Romano-Ward long QT syndrome. Analysis of 23 families.
    Towbin JA; Li H; Taggart RT; Lehmann MH; Schwartz PJ; Satler CA; Ayyagari R; Robinson JL; Moss A; Hejtmancik JF
    Circulation; 1994 Dec; 90(6):2635-44. PubMed ID: 7994803
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.