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 *

86 related articles for article (PubMed ID: 32152242)

  • 21. Janus kinase 3 missense mutation in a child with Jacobsen syndrome.
    Lotz DR; Knutsen AP
    Ann Allergy Asthma Immunol; 2010 Jun; 104(6):536-7. PubMed ID: 20568388
    [No Abstract]   [Full Text] [Related]  

  • 22. 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]  

  • 23. Jacobsen syndrome with bilateral periventricular white matter lesions.
    Lee HJ; Lee HI; Na JH; Lee YM
    World J Pediatr; 2022 Feb; 18(2):142-143. PubMed ID: 34860330
    [No Abstract]   [Full Text] [Related]  

  • 24. Hypoimmunoglobulinemia and protein C deficiency in a girl with Jacobsen syndrome: a case report.
    Sinawat S; Kitkhuandee A; Auvichayapat N; Auvichayapat P; Yospaiboon Y; Sinawat S
    J Med Assoc Thai; 2013 Jul; 96(7):870-3. PubMed ID: 24319861
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Sleep problems in individuals with 11q terminal deletion disorder (Jacobsen syndrome).
    Maas AP; Grossfeld PD; Didden R; Korzilius H; Braam WJ; Smits MG; Curfs LM
    Genet Couns; 2008; 19(2):225-35. PubMed ID: 18618998
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Paris-Trousseau-type macrothrombocytopenia without 11q deletion.
    Kaya Z; Kocak U; Perçin F; Kunishima S; Albayrak M; Gursel T; Ozogul C
    Pediatr Int; 2010 Apr; 52(2):e67-71. PubMed ID: 20500464
    [No Abstract]   [Full Text] [Related]  

  • 27. 11q23 deletion syndrome (Jacobsen syndrome) with severe bleeding: a case report.
    Ichimiya Y; Wada Y; Kunishima S; Tsukamoto K; Kosaki R; Sago H; Ishiguro A; Ito Y
    J Med Case Rep; 2018 Jan; 12(1):3. PubMed ID: 29307309
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Immunodeficiency and Lymphoma in Jacobsen Syndrome.
    Nigolian H; Nieke JP; Chevallier M; Stathaki E; Sloan-Béna F; Carminho-Rodrigues MT; Jandus P
    J Investig Allergol Clin Immunol; 2022 Oct; 32(5):408-409. PubMed ID: 35029149
    [No Abstract]   [Full Text] [Related]  

  • 29. Morphological and genetic abnormalities in a Jacobsen syndrome.
    Jurcă AD; Kozma K; Ioana M; Streaţă I; Petcheşi CD; Bembea M; Jurcă MC; Cuc EA; Vesa CM; Buhaş CL
    Rom J Morphol Embryol; 2017; 58(4):1531-1534. PubMed ID: 29556653
    [TBL] [Abstract][Full Text] [Related]  

  • 30. De novo interstitial deletion in the long arm of chromosome 11: a case report.
    Li LL; Zhang HG; Shao XG; Gao JC; Zhang HY; Liu RZ
    Genet Mol Res; 2016 Jul; 15(2):. PubMed ID: 27421024
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Chromosomal microarray mapping suggests a role for BSX and Neurogranin in neurocognitive and behavioral defects in the 11q terminal deletion disorder (Jacobsen syndrome).
    Coldren CD; Lai Z; Shragg P; Rossi E; Glidewell SC; Zuffardi O; Mattina T; Ivy DD; Curfs LM; Mattson SN; Riley EP; Treier M; Grossfeld PD
    Neurogenetics; 2009 Apr; 10(2):89-95. PubMed ID: 18855024
    [TBL] [Abstract][Full Text] [Related]  

  • 32. FEVR-like Presentation in an 11q Deletion Syndrome and 16p13.11 Microdeletion.
    Garcia MD; Ventura CV; Berrocal AM
    J Pediatr Ophthalmol Strabismus; 2017 Nov; 54():e71-e74. PubMed ID: 29156058
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Two siblings with 11qter deletion syndrome that had been rescued in their mother by uniparental disomy.
    Kawai M; Tsutsumi M; Suzuki F; Sameshima K; Dowa Y; Kyoya T; Inagaki H; Kurahashi H
    Eur J Med Genet; 2019 Mar; 62(3):224-228. PubMed ID: 30031150
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A case with 46,XX,del(11)(q23.2) karyotype and poor vision with literature review.
    Mahjoubi F; Razazian F; Torabi R
    Genet Couns; 2014; 25(3):277-87. PubMed ID: 25365850
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Prenatal diagnosis of mosaicism for 11q terminal deletion.
    Valduga M; Cannard VL; Philippe C; Romana S; Miton A; Droulle P; Foliguet B; Lecompte T; Jonveaux P
    Eur J Med Genet; 2007; 50(6):475-81. PubMed ID: 17761465
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A de novo 11q23 deletion in a patient presenting with severe ophthalmologic findings, psychomotor retardation and facial dysmorphism.
    Şimşek-Kiper PÖ; Bayram Y; Ütine GE; Alanay Y; Boduroğlu K
    Turk J Pediatr; 2014; 56(1):80-4. PubMed ID: 24827952
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 11q terminal deletion disorder and common variable immunodeficiency.
    Puglisi G; Netravali MA; MacGinnitie AJ; Bonagura VR
    Ann Allergy Asthma Immunol; 2009 Sep; 103(3):267-8. PubMed ID: 19788026
    [No Abstract]   [Full Text] [Related]  

  • 38. 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]  

  • 39. [Prenatal diagnosis of Jacobsen syndrome in a fetus carried by a pregnant woman with intellectual disability].
    Guo C; Wang J; Tang Y; Shi H; Liu J; Zhao L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Aug; 36(8):826-288. PubMed ID: 31400138
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Diagnosis and fine mapping of a deletion in distal 11q in two Chinese patients with developmental delay.
    Ji T; Wu Y; Wang H; Wang J; Jiang Y
    J Hum Genet; 2010 Aug; 55(8):486-9. PubMed ID: 20520618
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.