BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

140 related articles for article (PubMed ID: 8486353)

  • 21. Cytogenetic, FISH and array-CGH characterization of a complex chromosomal rearrangement carried by a mentally and language impaired patient.
    Ballarati L; Recalcati MP; Bedeschi MF; Lalatta F; Valtorta C; Bellini M; Finelli P; Larizza L; Giardino D
    Eur J Med Genet; 2009; 52(4):218-23. PubMed ID: 19236961
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Molecular cloning and physical and genetic mapping of the human anion exchanger isoform 3 (SLC2C) gene to chromosome 2q36.
    Su YR; Klanke CA; Houseal TW; Linn SC; Burk SE; Varvil TS; Otterud BE; Shull GE; Leppert MF; Menon AG
    Genomics; 1994 Aug; 22(3):605-9. PubMed ID: 8001971
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Identification of the breakpoint-flanking markers on chromosomes 1 and 17 of a constitutional translocation T(1;17)(P36;Q12-21) in a patient with neuroblastoma].
    Laureys GG
    Verh K Acad Geneeskd Belg; 1995; 57(5):389-422. PubMed ID: 8571670
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Finding the gene(s) for Waardenburg syndrome(s).
    Grundfast KM; San Agustin TB
    Otolaryngol Clin North Am; 1992 Oct; 25(5):935-51. PubMed ID: 1408197
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Normal hearing in Splotch (Sp/+), the mouse homologue of Waardenburg syndrome type 1.
    Steel KP; Smith RJ
    Nat Genet; 1992 Sep; 2(1):75-9. PubMed ID: 1303254
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Index, comprehensive microsatellite, and unified linkage maps of human chromosome 14 with cytogenetic tie points and a telomere microsatellite marker.
    Pandit SD; Wang JC; Veile RA; Mishra SK; Warlick CA; Donis-Keller H
    Genomics; 1995 Oct; 29(3):653-64. PubMed ID: 8575758
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Waardenburg's syndrome].
    Cacheux V; Delezoide AL; Vekemans M
    C R Seances Soc Biol Fil; 1996; 190(5-6):577-80. PubMed ID: 9074723
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Subchromosomal band interval mapping and ordering of DNA markers in the region 3q26.3-q27 involved in the dup(3q) syndrome.
    Rizzu P; Baldini A
    Genomics; 1994 Dec; 24(3):580-2. PubMed ID: 7713511
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Determination and regional assignment of grouped sets of microclones in chromosome 1pter-p35.
    Barnas CM; Onyango P; Ellmeier W; Lengauer C; Kleiner E; Henn T; Brunner C; Stapleton P; Weith A
    Genomics; 1995 Oct; 29(3):607-15. PubMed ID: 8575752
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Myelomeningocele and Waardenburg syndrome (type 3) in patients with interstitial deletions of 2q35 and the PAX3 gene: possible digenic inheritance of a neural tube defect.
    Nye JS; Balkin N; Lucas H; Knepper PA; McLone DG; Charrow J
    Am J Med Genet; 1998 Feb; 75(4):401-8. PubMed ID: 9482647
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Inverted duplications are recurrent rearrangements always associated with a distal deletion: description of a new case involving 2q.
    Bonaglia MC; Giorda R; Poggi G; Raggi ME; Rossi E; Baroncini A; Giglio S; Borgatti R; Zuffardi O
    Eur J Hum Genet; 2000 Aug; 8(8):597-603. PubMed ID: 10951522
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A genetic linkage map with 16 RFLP loci on the distal long arm of human chromosome 6.
    Saito S; Nakamura Y
    Genomics; 1993 Jan; 15(1):103-6. PubMed ID: 8094366
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Construction of a gene map of the nephronophthisis type 1 (NPHP1) region on human chromosome 2q12-q13.
    Nothwang HG; Stubanus M; Adolphs J; Hanusch H; Vossmerbäumer U; Denich D; Kübler M; Mincheva A; Lichter P; Hildebrandt F
    Genomics; 1998 Jan; 47(2):276-85. PubMed ID: 9479500
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Regional mapping of loci from human chromosome 2q to sheep chromosome 2q.
    Ansari HA; Pearce PD; Maher DW; Malcolm AA; Wood NJ; Phua SH; Broad TE
    Genomics; 1994 Mar; 20(1):122-4. PubMed ID: 8020939
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Atypical manifestations in familial type 1 Waardenburg syndrome].
    Sans B; Calvas P; Bazex J
    Ann Dermatol Venereol; 1998 Jan; 125(1):37-41. PubMed ID: 9747206
    [TBL] [Abstract][Full Text] [Related]  

  • 36. CRK proto-oncogene maps to human chromosome band 17p13.
    Fioretos T; Heisterkamp N; Groffen J; Benjes S; Morris C
    Oncogene; 1993 Oct; 8(10):2853-5. PubMed ID: 8378094
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Diagnosis and penetrance of dystopia canthorum in Waardenburg syndrome type I (WS1).
    Arias S
    Am J Med Genet; 1984 Apr; 17(4):863-7. PubMed ID: 6720753
    [No Abstract]   [Full Text] [Related]  

  • 38. A physical, transcript, and deletion map of chromosome region 12p12.3 flanked by ETV6 and CDKN1B: hypermethylation of the LRP6 CpG island in two leukemia patients with hemizygous del(12p).
    Baens M; Wlodarska I; Corveleyn A; Hoornaert I; Hagemeijer A; Marynen P
    Genomics; 1999 Feb; 56(1):40-50. PubMed ID: 10036184
    [TBL] [Abstract][Full Text] [Related]  

  • 39. High-resolution genetic map of the human glutamyl aminopeptidase gene (ENPEP).
    Li L; Wu Q; Barnoski BL; Cooper MD
    Genomics; 1997 Aug; 43(3):380-3. PubMed ID: 9268642
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Closing in on the BPES gene on 3q23: mapping of a de Novo reciprocal translocation t(3;4)(q23;p15.2) breakpoint within a 45-kb cosmid and mapping of three candidate genes, RBP1, RBP2, and beta'-COP, distal to the breakpoint.
    De Baere E; Van Roy N; Speleman F; Fukushima Y; De Paepe A; Messiaen L
    Genomics; 1999 Apr; 57(1):70-8. PubMed ID: 10191085
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.