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 *

107 related articles for article (PubMed ID: 27735809)

  • 61. [Bilateral pulmonary artery banding for complex congenital heart disease in a patient with trisomy 13; report of a case].
    Maekawa Y; Yoshimura Y; Uchida T; Kim C; Miyazaki R; Ohba E; Nakamura K; Sadahiro M; Suzuki H; Otagiri T; Satoh M; Honma N
    Kyobu Geka; 2013 Jul; 66(7):585-8. PubMed ID: 23917139
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Type 1 diabetes mellitus associated with autoimmune thyroid disease, celiac disease and familial Mediterranean fever: case report.
    Baş F; Kabataş-Eryilmaz S; Günöz H; Darendeliler F; Küçükemre B; Bundak R; Saka N
    Turk J Pediatr; 2009; 51(2):183-6. PubMed ID: 19480334
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Prenatally detected trisomy 7 mosaicism in a dysmorphic child.
    Kivirikko S; Salonen R; Salo A; von Koskull H
    Prenat Diagn; 2002 Jul; 22(7):541-4. PubMed ID: 12124684
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Hypomelanosis of Ito presenting with unilateral dilation of Virchow-Robin spaces: a case report.
    Uçar Çİ; Yıldırım M; Sayar Y; Şahin S; Teber ST
    Childs Nerv Syst; 2021 Sep; 37(9):2931-2934. PubMed ID: 33585955
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Anodontia totalis fetalis in a trisomy 13 mosaic.
    Sperber GH; Honore LH
    J Dent Assoc S Afr; 1988 Nov; 43(11):543-6. PubMed ID: 3272969
    [No Abstract]   [Full Text] [Related]  

  • 66. A TRISOMY 13 CASE PRESENTING WITH CONGENITAL DIAPHRAGMATIC HERNIA AND MICROPHTHALMIA.
    Sahin S; Kutman KH; Bozkurt O; Canpolat FE; Uras N; Oguz SS; Topcu V; Ozdemir O; Dilmen U
    Genet Couns; 2015; 26(2):263-5. PubMed ID: 26349200
    [No Abstract]   [Full Text] [Related]  

  • 67. Multiorgan autoimmunity in a Turner syndrome patient with partial monosomy 2q and trisomy 10p.
    Grossi A; Palma A; Zanni G; Novelli A; Loddo S; Cappa M; Fierabracci A
    Gene; 2013 Feb; 515(2):439-43. PubMed ID: 23262341
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Prevalence of celiac disease in patients with autoimmune thyroiditis.
    Iuorio R; Mercuri V; Barbarulo F; D'Amico T; Mecca N; Bassotti G; Pietrobono D; Gargiulo P; Picarelli A
    Minerva Endocrinol; 2007 Dec; 32(4):239-43. PubMed ID: 18091661
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Monozygotic twins discordant for trisomy 13.
    Ramsey KW; Slavin TP; Graham G; Hirata GI; Balaraman V; Seaver LH
    J Perinatol; 2012 Apr; 32(4):306-8. PubMed ID: 22460600
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Trisomy 13: Changing Perspectives.
    Macias G; Riley C
    Neonatal Netw; 2016; 35(1):31-6. PubMed ID: 26842537
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Autoimmune thyroiditis in a case of 18p- syndrome.
    Gluckman PD
    Aust Paediatr J; 1977 Jun; 13(2):122-4. PubMed ID: 578739
    [No Abstract]   [Full Text] [Related]  

  • 72. A Family's Experience with Perinatal Palliative Care.
    Nordin TA; Clark EC
    Am Fam Physician; 2015 Apr; 91(7):442. PubMed ID: 25884742
    [No Abstract]   [Full Text] [Related]  

  • 73. Pigmentary mosaicism with mosaic chromosome 5p tetrasomy.
    Hansen LK; Brandrup F; Rasmussen K
    Br J Dermatol; 2003 Aug; 149(2):414-6. PubMed ID: 12932254
    [TBL] [Abstract][Full Text] [Related]  

  • 74. A toddler with phylloid-type pigmentary mosaicism and ambiguous genitalia resulting from trisomy 14 induced by a der(Y)t(Y;14).
    Romero VI; Pozo JC; Saenz S; Llamos-Paneque A; Liehr T; Hosomichi K; Tajima A
    Hum Genome Var; 2020; 7():28. PubMed ID: 33062287
    [TBL] [Abstract][Full Text] [Related]  

  • 75. "Choosing the road less traveled".
    Farlow B
    Curr Probl Pediatr Adolesc Health Care; 2011 Apr; 41(4):115-6. PubMed ID: 21440230
    [No Abstract]   [Full Text] [Related]  

  • 76. [ABNORMAL PATTERNS OF HEMOGLOBIN AND INTRA-ERYTHROCYTE ENZYMES IN A CASE OF D1 TRISOMY SYNDROME].
    IUCHI I; KAWAMURA J; YANAGIZAWA S; NAKASHIMA K; KASAHARA T; SHIBATA S
    Igaku To Seibutsugaku; 1965 Aug; 71():121-6. PubMed ID: 14345690
    [No Abstract]   [Full Text] [Related]  

  • 77. Hypomelanosis of Ito with gynaecomastia and dental anomaly.
    Gupta M; Gupta P; Sharma R; Gupta A
    BMJ Case Rep; 2018 Jul; 2018():. PubMed ID: 29982187
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Cortical visual impairment in hypomelanosis of Ito.
    Scott A; Micallef C; Hale SL; Watts P
    J Pediatr Ophthalmol Strabismus; 2008; 45(4):240-1. PubMed ID: 18705622
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Trisomy 12p mosaicism syndrome in a patient with hypopigmented cutaneous mosaicism and three cell lines in peripheral blood.
    Porcar Saura S; Díaz Giménez M; Guillén-Climent S; Villar C; Ruiz Quilez A; Abellán Sanchez MR; Cuesta Peredo A; Martín JM
    J Eur Acad Dermatol Venereol; 2023 Jan; 37(1):e54-e58. PubMed ID: 35993792
    [No Abstract]   [Full Text] [Related]  

  • 80. Postzygotic inactivating mutation of KIF13A located at chromosome 6p22.3 in a patient with a novel mosaic neuroectodermal syndrome.
    Lam CW; Chan CY; Wong KC; Chang ST
    J Hum Genet; 2021 Aug; 66(8):825-829. PubMed ID: 33526817
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.