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 *

214 related articles for article (PubMed ID: 7512788)

  • 21. Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization.
    Blennow E; Nielsen KB; Telenius H; Carter NP; Kristoffersson U; Holmberg E; Gillberg C; Nordenskjöld M
    Am J Med Genet; 1995 Jan; 55(1):85-94. PubMed ID: 7702104
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Interstitial deletion of 8q13.3-->22.1 associated with craniosynostosis.
    Fryburg JS; Golden WL
    Am J Med Genet; 1993 Mar; 45(5):638-41. PubMed ID: 7681252
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Identification of a supernumerary marker derived from chromosome 17 using FISH.
    Rosenberg C; Borovik CL; Canonaco RS; Sichero LC; Queiroz AP; Vianna-Morgante AM
    Am J Med Genet; 1995 Oct; 59(1):33-5. PubMed ID: 8849006
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Fluorescence in situ hybridization in 6 patients with alterations of chromosome 18 and in 7 with marker chromosomes].
    Esmer MC; Carnevale A; Gómez L; del Castillo V; Frías S
    Rev Invest Clin; 1996; 48(1):27-33. PubMed ID: 8815483
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Developmental delay, short stature, and minor facial anomalies in a child with ring chromosome 16.
    Chodirker BN; Ray M; McAlpine PJ; Riordan D; Vust A; Pugh D; Chudley AE
    Am J Med Genet; 1988 Sep; 31(1):145-51. PubMed ID: 2464927
    [TBL] [Abstract][Full Text] [Related]  

  • 26. M-banding characterization of a 16p11.2p13.1 tandem duplication in a child with autism, neurodevelopmental delay and dysmorphism.
    Behjati F; Shafaghati Y; Firouzabadi SG; Kahrizi K; Bagherizadeh I; Najmabadi H; Bint S; Ogilvie C
    Eur J Med Genet; 2008; 51(6):608-14. PubMed ID: 18674645
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Lack of expression of XIST from a small ring X chromosome containing the XIST locus in a girl with short stature, facial dysmorphism and developmental delay.
    Tomkins DJ; McDonald HL; Farrell SA; Brown CJ
    Eur J Hum Genet; 2002 Jan; 10(1):44-51. PubMed ID: 11896455
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Mosaic r(13) resulting in large deletion of chromosome 13q in a newborn female with multiple congenital anomalies.
    Lorentz CP; Jalal SM; Thompson DM; Babovic-Vuksanovic D
    Am J Med Genet; 2002 Jul; 111(1):61-7. PubMed ID: 12124737
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Supernumerary marker chromosomes 5: confirmation of a critical region and resultant phenotype.
    D'Amato Sizonenko L; Ng D; Oei P; Winship I
    Am J Med Genet; 2002 Jul; 111(1):19-26. PubMed ID: 12124728
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Array-CGH and clinical findings in a patient with a small supernumerary r(8) mosaicism.
    Eyüpoğlu FC; Sünnetçi D; Cine N; Savli H; Okten A; Açikgöz EG; Sönmez FM
    Genet Couns; 2014; 25(3):305-13. PubMed ID: 25365853
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Detection of an unbalanced t(4;15) by FISH in a child with multiple congenital anomalies.
    Celep F; Acar H; Aynaci O; Aynaci FM; Karagüzel A
    Genet Couns; 2001; 12(4):319-26. PubMed ID: 11837600
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Interstitial duplication 19p.
    Stratton RF; DuPont BR; Olsen AS; Fertitta A; Hoyer M; Moore CM
    Am J Med Genet; 1995 Jul; 57(4):562-4. PubMed ID: 7573129
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Cytogenetic and molecular identification of a de novo direct duplication of the long arm of chromosome 4(q21.3-->q31.3).
    Jeziorowska A; Ciesla W; Houck GE; Yao XL; Harris MS; Truszczak B; Skorski M; Jakubowski L; Jenkins EC; Kaluzewski B
    Am J Med Genet; 1993 Apr; 46(1):83-7. PubMed ID: 7684191
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Ring chromosome 8: microcephaly, mental retardation and minor facial anomalies with adhesive behavioral phenotype].
    Bibas Bonet H; Fontenla M; Fauze R; G de Pinat I
    Rev Neurol; 2001 Apr 16-30; 32(8):746-50. PubMed ID: 11391511
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Ring chromosome 8 associated with microcephaly.
    Mingarelli R; Valorani G; Zelante L; Dallapiccola B
    Ann Genet; 1991; 34(2):90-2. PubMed ID: 1746890
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Ring chromosome 22 and autism: report and review.
    MacLean JE; Teshima IE; Szatmari P; Nowaczyk MJ
    Am J Med Genet; 2000 Feb; 90(5):382-5. PubMed ID: 10706359
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Small familial supernumerary ring chromosome 2: FISH characterization and genotype-phenotype correlation.
    Giardino D; Finelli P; Russo S; Gottardi G; Rodeschini O; Atza MG; Natacci F; Larizza L
    Am J Med Genet; 2002 Aug; 111(3):319-23. PubMed ID: 12210331
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Cryptic 6q subtelomeric deletion associated with a paracentric inversion in a mildly retarded child.
    Lorda-Sanchez I; Lopez-Pajares I; Roche MC; Sanz R; Rodriguez de Alba M; Gonzalez-Gonzalez MC; Ibañez A; Ramos C; Ayuso C
    Am J Med Genet; 2000 Dec; 95(4):336-8. PubMed ID: 11186887
    [TBL] [Abstract][Full Text] [Related]  

  • 39. De novo mosaic ring chromosome 18 in a child with mental retardation, epilepsy and immunological problems.
    Lo-Castro A; El-Malhany N; Galasso C; Verrotti A; Nardone AM; Postorivo D; Palmieri C; Curatolo P
    Eur J Med Genet; 2011; 54(3):329-32. PubMed ID: 21333764
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Marker chromosome 21 identified by microdissection and FISH.
    Sun Y; Rubinstein J; Soukup S; Palmer CG
    Am J Med Genet; 1995 Mar; 56(2):151-4. PubMed ID: 7542834
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.