BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

422 related articles for article (PubMed ID: 11043435)

  • 1. A case with 47,XXY,del(11)(q23) karotype-coexistence of Jacobsen and Klinefelter syndromes.
    Matheisel A; Babinska M; Wierzba J; Wozniak A; Nedoszytko B; Balcerska A; Limon J
    Genet Couns; 2000; 11(3):267-71. PubMed ID: 11043435
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Beckwith-Wiedemann syndrome due to 11p15.5 paternal duplication associated with Klinefelter syndrome and a "de novo" pericentric inversion of chromosome Y.
    Delicado A; Lapunzina P; Palomares M; Molina MA; Galán E; López Pajares I
    Eur J Med Genet; 2005; 48(2):159-66. PubMed ID: 16053907
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Clinical picture of partial monosomy of chromosome 11 q].
    Dörr U
    Monatsschr Kinderheilkd; 1986 Nov; 134(11):808-11. PubMed ID: 3807920
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Coexistent mosaic monosomy 21 and fragile X syndrome in a mentally retarded male patient.
    Utine GE; Aktas D; Boduroğlu K; Alikasifoğlu M; Tunçbilek E
    Genet Couns; 2007; 18(2):171-7. PubMed ID: 17710869
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Precocious puberty associated with partial trisomy 18q and monosomy 11q.
    Mutesa L; Hellin AC; Jamar M; Pierquin G; Bours V; Verloes A
    Genet Couns; 2007; 18(2):201-7. PubMed ID: 17710872
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
    Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
    Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Jacobsen syndrome: chromosome deletion at 11q23.
    Clang DR; LaBaere RJ
    J Am Osteopath Assoc; 1998 Oct; 98(10):551-4. PubMed ID: 9821738
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Supernumerary chromosome der(22)t(11;22): Emanuel syndrome associates with novel features.
    Yosunkaya Fenerci E; Guven GS; Kuru D; Yilmaz S; Tarkan-Argüden Y; Cirakoglu A; Deviren A; Yüksel A; Hacihanefioğlu S
    Genet Couns; 2007; 18(4):401-8. PubMed ID: 18286821
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 18q- and 18q+ mosaicism in a mentally retarded boy.
    Ausems MG; Bhola SL; Post-Blok CA; Hennekam RC; de France HF
    Am J Med Genet; 1994 Nov; 53(3):296-9. PubMed ID: 7856666
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Deletion 11q23-->qter (Jacobsen syndrome). Report of three new patients.
    Obregon MG; Mingarelli R; Digilio MC; Zelante L; Giannotti A; Sabatino G; Dallapiccola B
    Ann Genet; 1992; 35(4):208-12. PubMed ID: 1296516
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A de novo subtelomeric monosomy 11q (11q24.2-qter) and trisomy 20q (20q13.3-qter) in a girl with findings compatible with Jacobsen syndrome: case report and review.
    Courtens W; Wauters J; Wojciechowski M; Reyniers E; Scheers S; van Luijk R; Rooms L; Kooy F; Wuyts W
    Clin Dysmorphol; 2007 Oct; 16(4):231-9. PubMed ID: 17786114
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Double aneuploidy in three Egyptian patients: Down-Turner and Down-Klinefelter syndromes.
    Zaki MS; Kamel AA; El-Ruby M
    Genet Couns; 2005; 16(4):393-402. PubMed ID: 16440882
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A variant Klinefelter syndrome patient with an XXY/XX/XY karyotype studied by GTG-banding and fluorescence in situ hybridization.
    Mark HF; Bai H; Sotomayor E; Mark S; Zolnierz K; Airall E; Sigman M
    Exp Mol Pathol; 1999 Sep; 67(1):50-6. PubMed ID: 10493892
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Distal 11q monosomy syndrome: a report of two Egyptian sibs with normal parental karyotypes confirmed by molecular cytogenetics.
    Afifi HH; Zaki MS; El-Gerzawy AM; Kayed HF
    Genet Couns; 2008; 19(1):47-58. PubMed ID: 18564501
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Partial monosomy of chromosome 2. Delineable syndrome of deletion 2 (q23-q31).
    Shabtai F; Klar D; Halbrecht I
    Ann Genet; 1982; 25(3):156-8. PubMed ID: 6982665
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Deletion 11q23 --> qter (Jacobsen Syndrome) associated with duodenal atresia and annular pancreas].
    Fernández González N; Prieto Espuñes S; Ibáñez Fernández A; Fernández Colomer B; López Sastre J; Fernández Toral J
    An Esp Pediatr; 2002 Sep; 57(3):249-52. PubMed ID: 12199949
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A small deletion of 16q23.1-->16q24.2 [del(16)(q23.1q24.2).ish del(16)(q23.1q24.2)(D16S395+, D16S348-, P5432+)] in a boy with iris coloboma and minor anomalies.
    Werner W; Kraft S; Callen DF; Bartsch O; Hinkel GK
    Am J Med Genet; 1997 Jun; 70(4):371-6. PubMed ID: 9182777
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Del(4)(pter-->q33:) case report and review of the literature.
    Grammatico P; Spaccini L; Di Rosa C; Cupilari F; Del Porto G
    Genet Couns; 1997; 8(1):39-42. PubMed ID: 9101277
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mosaic status in lymphocytes of infertile men with or without Klinefelter syndrome.
    Lenz P; Luetjens CM; Kamischke A; Kühnert B; Kennerknecht I; Nieschlag E
    Hum Reprod; 2005 May; 20(5):1248-55. PubMed ID: 15665007
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Jacobsen syndrome without thrombocytopenia: a case report and review of the literature.
    Nalbantoğlu B; Donma MM; Nişli K; Paketçi C; Karasu E; Ozdilek B; Mintaş NE
    Turk J Pediatr; 2013; 55(2):203-6. PubMed ID: 24192682
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.