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Journal Abstract Search

170 related items for PubMed ID: 22842076

  • 1. A de novo 4.4-Mb microdeletion in 2p24.3 → p24.2 in a girl with bilateral hearing impairment, microcephaly, digit abnormalities and Feingold syndrome.
    Chen CP, Lin SP, Chern SR, Wu PS, Chang SD, Ng SH, Liu YP, Su JW, Wang W.
    Eur J Med Genet; 2012 Nov; 55(11):666-9. PubMed ID: 22842076
    [Abstract] [Full Text] [Related]

  • 2. Features of Feingold syndrome 1 dominate in subjects with 2p deletions including MYCN.
    Burnside RD, Molinari S, Botti C, Brooks SS, Chung WK, Mehta L, Schwartz S, Papenhausen P.
    Am J Med Genet A; 2018 Sep; 176(9):1956-1963. PubMed ID: 30088856
    [Abstract] [Full Text] [Related]

  • 3. GENETIC COUNSELLING IN FEINGOLD SYNDROME AND A NOVEL MUTATION.
    Atik T, Güvenç MS, Onay H, Özkinay F, Çoğulu Ö.
    Genet Couns; 2016 Sep; 27(3):381-384. PubMed ID: 30204967
    [Abstract] [Full Text] [Related]

  • 4. De novo 13q31.1-q32.1 interstitial deletion encompassing the miR-17-92 cluster in a patient with Feingold syndrome-2.
    Tassano E, Di Rocco M, Signa S, Gimelli G.
    Am J Med Genet A; 2013 Apr; 161A(4):894-6. PubMed ID: 23495052
    [No Abstract] [Full Text] [Related]

  • 5. Feingold syndrome type 2 in a patient from China.
    Lei J, Han L, Huang Y, Long M, Zhao G, Yan S, Zhang J.
    Am J Med Genet A; 2021 Jul; 185(7):2262-2266. PubMed ID: 33818875
    [Abstract] [Full Text] [Related]

  • 6. A case of Feingold type 2 syndrome associated with keratoconus refines keratoconus type 7 locus on chromosome 13q.
    Sirchia F, Di Gregorio E, Restagno G, Grosso E, Pappi P, Talarico F, Savin E, Cavalieri S, Giorgio E, Mancini C, Pasini B, Mehta JS, Brusco A.
    Eur J Med Genet; 2017 Apr; 60(4):224-227. PubMed ID: 28159702
    [Abstract] [Full Text] [Related]

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  • 8. A novel mutation in MYCN gene causing congenital absence of the flexor pollicis longus tendon as an unusual presentation of Feingold syndrome 1.
    Peleg A, Kurolap A, Sagi-Dain L, Larom-Khan G, Adir V, Mory A, Paperna T, Shuldiner AR, Gonzaga-Jauregui C, Adir N, Baris Feldman H, Wollstein R.
    Clin Dysmorphol; 2021 Apr 01; 30(2):71-75. PubMed ID: 32925198
    [Abstract] [Full Text] [Related]

  • 9. Growth hormone deficiency, aortic dilation, and neurocognitive issues in Feingold syndrome 2.
    Muriello M, Kim AY, Sondergaard Schatz K, Beck N, Gunay-Aygun M, Hoover-Fong JE.
    Am J Med Genet A; 2019 Mar 01; 179(3):410-416. PubMed ID: 30672094
    [Abstract] [Full Text] [Related]

  • 10. A fourth case of Feingold syndrome type 2: psychiatric presentation and management.
    Ganjavi H, Siu VM, Speevak M, MacDonald PA.
    BMJ Case Rep; 2014 Nov 12; 2014():. PubMed ID: 25391829
    [Abstract] [Full Text] [Related]

  • 11. Metacarpophalangeal pattern profile analysis for a 3-month-old infant with Feingold syndrome 2.
    Isobe A, Maeda N, Fujita H, Banno S, Kageyama T, Hatabu N, Sato R, Suzuki E, Miharu M, Komiyama O, Nakashima M, Matsunaga T, Nishimura G, Yamazawa K.
    Am J Med Genet A; 2021 Mar 12; 185(3):952-954. PubMed ID: 33369046
    [No Abstract] [Full Text] [Related]

  • 12. Dissection of the MYCN locus in Feingold syndrome and isolated oesophageal atresia.
    Cognet M, Nougayrede A, Malan V, Callier P, Cretolle C, Faivre L, Genevieve D, Goldenberg A, Heron D, Mercier S, Philip N, Sigaudy S, Verloes A, Sarnacki S, Munnich A, Vekemans M, Lyonnet S, Etchevers H, Amiel J, de Pontual L.
    Eur J Hum Genet; 2011 May 12; 19(5):602-6. PubMed ID: 21224895
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  • 14. A Novel MYCN Variant Associated with Intellectual Disability Regulates Neuronal Development.
    Yu X, Hu L, Liu X, Zhan G, Mei M, Wang H, Zhang X, Qiu Z, Zhou W, Yang L.
    Neurosci Bull; 2018 Oct 12; 34(5):854-858. PubMed ID: 29786759
    [No Abstract] [Full Text] [Related]

  • 15. A Feingold syndrome case with previously undescribed features and a new mutation.
    Koçak H, Ozaydin E, Köse G, Marcelis CL, Kamsteeg EJ, Ceylaner S.
    Genet Couns; 2009 Oct 12; 20(3):261-7. PubMed ID: 19852433
    [Abstract] [Full Text] [Related]

  • 16. A de novo 13q31.3 microduplication encompassing the miR-17 ~ 92 cluster results in features mirroring those associated with Feingold syndrome 2.
    Siavrienė E, Preikšaitienė E, Maldžienė Ž, Mikštienė V, Rančelis T, Ambrozaitytė L, Gueneau L, Reymond A, Kučinskas V.
    Gene; 2020 Aug 30; 753():144816. PubMed ID: 32473250
    [Abstract] [Full Text] [Related]

  • 17. Distinct molecular pathways mediate Mycn and Myc-regulated miR-17-92 microRNA action in Feingold syndrome mouse models.
    Mirzamohammadi F, Kozlova A, Papaioannou G, Paltrinieri E, Ayturk UM, Kobayashi T.
    Nat Commun; 2018 Apr 10; 9(1):1352. PubMed ID: 29636449
    [Abstract] [Full Text] [Related]

  • 18. Detection of a de novo interstitial 2q microdeletion by CGH microarray analysis in a patient with limb malformations, microcephaly and mental retardation.
    Svensson AM, Curry CJ, South ST, Whitby H, Maxwell TM, Aston E, Fisher J, Carmack CE, Scheffer A, Abu-Shamsieh A, Brothman AR.
    Am J Med Genet A; 2007 Jun 15; 143A(12):1348-53. PubMed ID: 17506097
    [Abstract] [Full Text] [Related]

  • 19. How many entities exist for the spectrum of disorders associated with brachydactyly, syndactyly, short stature, microcephaly, and intellectual disability?
    Ravel A, Chouery E, Stora S, Jalkh N, Villard L, Temtamy S, Mégarbané A.
    Am J Med Genet A; 2011 Apr 15; 155A(4):880-4. PubMed ID: 21416592
    [Abstract] [Full Text] [Related]

  • 20. [Association esophageal atresia type 3 - microcephaly: an incomplete Feingold syndrome?].
    Shongo MY, Lubala TK, Mbuyi SM, Makinko PI, Ngwej DT, Kabange FN.
    Pan Afr Med J; 2012 Apr 15; 13():85. PubMed ID: 23396887
    [Abstract] [Full Text] [Related]

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