BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

67 related articles for article (PubMed ID: 7130958)

  • 21. Interstitial deletions of the short arm of chromosome 4 in patients with a similar combination of multiple minor anomalies and mental retardation.
    White DM; Pillers DA; Reiss JA; Brown MG; Magenis RE
    Am J Med Genet; 1995 Jul; 57(4):588-97. PubMed ID: 7573135
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Supernumerary inv dup(15) in a patient with Angelman syndrome and a deletion of 15q11-q13.
    Spinner NB; Zackai E; Cheng SD; Knoll JH
    Am J Med Genet; 1995 May; 57(1):61-5. PubMed ID: 7645601
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Deletions of different segments of the long arm of chromosome 4.
    Mitchell JA; Packman S; Loughman WD; Fineman RM; Zackai E; Patil SR; Emanual B; Bartley JA; Hanson JW
    Am J Med Genet; 1981; 8(1):73-89. PubMed ID: 7246608
    [TBL] [Abstract][Full Text] [Related]  

  • 24. De novo 10q22 interstitial deletion.
    Cook L; Weaver DD; Hartsfield JK; Vance GH
    J Med Genet; 1999 Jan; 36(1):71-2. PubMed ID: 9950372
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Mild mandibulofacial dysostosis in a child with a deletion of 3p.
    Arn PH; Mankinen C; Jabs EW
    Am J Med Genet; 1993 Jun; 46(5):534-6. PubMed ID: 8322816
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Heterozygosity mapping by quantitative fluorescent PCR reveals an interstitial deletion in Xq26.2-q28 associated with ovarian dysfunction.
    Fimiani G; Laperuta C; Falco G; Ventruto V; D'Urso M; Ursini MV; Miano MG
    Hum Reprod; 2006 Feb; 21(2):529-35. PubMed ID: 16239311
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Ectrodactyly and proximal/intermediate interstitial deletion 7q.
    McElveen C; Carvajal MV; Moscatello D; Towner J; Lacassie Y
    Am J Med Genet; 1995 Mar; 56(1):1-5. PubMed ID: 7747769
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Use of fluorescence in situ hybridization to clarify a complex chromosomal rearrangement in a child with multiple congenital anomalies.
    Spikes AS; Hegmann K; Smith JL; Shaffer LG
    Am J Med Genet; 1995 May; 57(1):31-4. PubMed ID: 7645595
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Subtle overlapping deletions in the terminal region of chromosome 6q24.2-q26: three cases studied using FISH.
    Sukumar S; Wang S; Hoang K; Vanchiere CM; England K; Fick R; Pagon B; Reddy KS
    Am J Med Genet; 1999 Nov; 87(1):17-22. PubMed ID: 10528241
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Tentative localization of a Hageman (Factor XII) locus on 7q, probably the 7q35 band.
    de Grouchy J; Turleau C
    Humangenetik; 1974; 24(3):197-200. PubMed ID: 4140832
    [No Abstract]   [Full Text] [Related]  

  • 31. No chromosome deletion found on prometaphase banding in two cases of Langer-Giedion syndrome.
    Gorlin RJ; Cervenka J; Bloom BA; Langer LO
    Am J Med Genet; 1982 Nov; 13(3):345-7. PubMed ID: 6983832
    [No Abstract]   [Full Text] [Related]  

  • 32. Refined mapping of the gene for glutathione reductase on human chromosome 8.
    Gutensohn W; Rodewald A; Haas B; Schulz P; Cleve H
    Hum Genet; 1978 Aug; 43(2):221-4. PubMed ID: 689688
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Chromosome 6q- in metastatic melanoma involving the large bowel.
    Reichmann A; Martin P; Levin B
    Cancer Genet Cytogenet; 1984 Nov; 13(3):275-7. PubMed ID: 6498791
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A de novo interstitial deletion of band q21 on chromosome 6.
    Cote GB; Papadakou-Lagoyanni S; Metaxotou C
    Ann Genet; 1981; 24(3):170-1. PubMed ID: 6974529
    [No Abstract]   [Full Text] [Related]  

  • 35. Tentative assignment of piebald trait gene to chromosome band 4q12.
    Hoo JJ; Haslam RH; van Orman C
    Hum Genet; 1986 Jul; 73(3):230-1. PubMed ID: 3733079
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A patient with an interstitial deletion of the short arm of chromosome 6.
    van Swaay E; Beverstock GC; van de Kamp JJ
    Clin Genet; 1988 Feb; 33(2):95-101. PubMed ID: 3359674
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Interstitial deletion of chromosome 21.
    Modi N; Buckton KE
    Clin Genet; 1982 Oct; 22(4):215-9. PubMed ID: 7151306
    [No Abstract]   [Full Text] [Related]  

  • 38. Interstitial deletion of chromosome 7p detected antenatally.
    Marks K; Hill L; Chitham RG; Whitehouse WL
    J Med Genet; 1985 Aug; 22(4):316-8. PubMed ID: 4045964
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genetic analysis of human cell surface structures.
    Jones C
    Haematol Blood Transfus; 1979; 23():313-7. PubMed ID: 544365
    [No Abstract]   [Full Text] [Related]  

  • 40. Gene mapping by exclusion.
    Ferguson-Smith MA
    Birth Defects Orig Artic Ser; 1975; 11(3):126-9. PubMed ID: 1203470
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.