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 *

93 related articles for article (PubMed ID: 20235000)

  • 41. Rapid aneuploidy testing versus traditional karyotyping: is it better to know more?
    Leung TN
    Hong Kong Med J; 2008 Feb; 14(1):4-5. PubMed ID: 18239236
    [No Abstract]   [Full Text] [Related]  

  • 42. [Triploidy as a cause of midtrimester gestosis(author's transl)].
    Schinzel A; Hayashi K; Schmid W; Knecht B; Tuschy G; Boltshauser E
    Arch Gynakol; 1975; 218(2):113-23. PubMed ID: 1174023
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Genome-wide abnormalities in embryos: Origins and clinical consequences.
    Masset H; Tšuiko O; Vermeesch JR
    Prenat Diagn; 2021 Apr; 41(5):554-563. PubMed ID: 33524193
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Alobar holoprosencephaly and otocephaly in a female infant with a normal karyotype and placental villitis.
    Gaba AR; Anderson GJ; VanDyke DL; Chason JL
    J Med Genet; 1982 Feb; 19(1):78. PubMed ID: 7069754
    [No Abstract]   [Full Text] [Related]  

  • 45. A severe prenatal presentation of Cat Eye Syndrome.
    Jedraszak G; Receveur A; Andrieux J; Naepels P; Mathieu-Dramard M; Bremond-Gignac D; Sevestre H; Copin H; Rochette J
    Clin Dysmorphol; 2013 Oct; 22(4):175-177. PubMed ID: 23982124
    [No Abstract]   [Full Text] [Related]  

  • 46. Physical and psychomotor development of 1799 children born after second trimester amniocentesis for maternal serum positive triple test screening and normal prenatal karyotype.
    Witters I; Moerman P; Van Assche A; Fryns JP
    J Med Genet; 2002 Dec; 39(12):e75. PubMed ID: 12471213
    [No Abstract]   [Full Text] [Related]  

  • 47. CD68 immunostaining in the evaluation of chronic histiocytic intervillositis.
    Heller DS
    Arch Pathol Lab Med; 2012 Jun; 136(6):657-9. PubMed ID: 22646274
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Triploidy mosaicism (45,X/68,XX) in an infant presenting with failure to thrive.
    Posey JE; Mohrbacher N; Smith JL; Patel A; Potocki L; Breman AM
    Am J Med Genet A; 2016 Mar; 170(3):694-8. PubMed ID: 26566716
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [Fathoming of NIPT to further improve the efficiency of prenatal screening for birth defects].
    Hu YL; Yang HX
    Zhonghua Fu Chan Ke Za Zhi; 2020 Feb; 55(2):91-93. PubMed ID: 32146736
    [TBL] [Abstract][Full Text] [Related]  

  • 50. [Prenatal diagnosis of triploidy].
    Slezak R; Florjański J; Zalewski J; Sasiadek M; Heimrath J
    Ginekol Pol; 2005 Apr; 76(4):295-9. PubMed ID: 16013182
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Recurrent placental microcalcifications in the second trimester.
    Chia CC; Huang SC
    Taiwan J Obstet Gynecol; 2010 Sep; 49(3):357-8. PubMed ID: 21056323
    [No Abstract]   [Full Text] [Related]  

  • 52. Cromosoma 13 en anillo.
    Cammarata-Scalisi F; Briceño Y; Cegarra E; Montilla D
    Bol Med Hosp Infant Mex; 2019; 76(2):100-103. PubMed ID: 30907385
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Electroclinical characteristics and neuropsychological profile of a female child with chromosome 5p13.2 duplication syndrome.
    Lucarelli E; Pasca MG; Fanizza I; Trabacca A
    Neurol Sci; 2017 May; 38(5):915-917. PubMed ID: 28108830
    [No Abstract]   [Full Text] [Related]  

  • 54. Renal tubular dysgenesis complicated with severe cranium hypoplasia.
    Shirakawa T; Kondoh T; Takahashi R; Nakayama M; Kusumoto T; Matsudaira M; Nakashima Y; Kinoshita E; Miyamoto M; Masuzaki H; Uetani M; Nazneen A; Taguchi T; Moriuchi H
    Pediatr Int; 2004 Feb; 46(1):88-90. PubMed ID: 15043673
    [No Abstract]   [Full Text] [Related]  

  • 55. Mixoploidy combined with aneuploidy in a 13 year-old patient with severe multiple congenital abnormalities and intellectual disability.
    van Zutven LJCM; Mancini GMS; Bindels-de Heus KGCB; van den Akker ELT; Hulsman LOM; Smit M; Berna Beverloo H
    Am J Med Genet A; 2018 Feb; 176(2):492-495. PubMed ID: 29226581
    [No Abstract]   [Full Text] [Related]  

  • 56. Potocki-Lupski syndrome in conjunction with bilateral clubfoot.
    Dhanaraj D; Chu A; Pappas JG; Moran E; Lehman WB
    J Pediatr Orthop B; 2015 Jul; 24(4):373-6. PubMed ID: 25768679
    [TBL] [Abstract][Full Text] [Related]  

  • 57. A rare case of 68,XX triploidy diagnosed by amniocentesis.
    Kaffe S; Eliasen C; Wan L; Charles N; Jansen V; Greco MA; Hsu LY
    Prenat Diagn; 1989 Dec; 9(12):857-61. PubMed ID: 2626411
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [Results of clinical and genetic diagnosis of rare diseases in the Eastern region of Hungary (2007-2013)].
    Szakszon K; Balogh E; Ujfalusi A; Bessenyei B; P Szabó G; Balogh I; Oláh E
    Orv Hetil; 2014 Mar; 155(9):348-57. PubMed ID: 24566699
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Prenatal diagnosis of XYY karyotype.
    Dumars KW; Fialko G; Willis J
    Am J Dis Child; 1976 Nov; 130(11):1295-6. PubMed ID: 984014
    [No Abstract]   [Full Text] [Related]  

  • 60. Gastrointestinal manifestations in diploid/triploid mixoploidy.
    Lalani FK; Elsner GL; Lebel RR; Beg MB
    J Pediatr Gastroenterol Nutr; 2015 Jun; 60(6):799-801. PubMed ID: 25373857
    [TBL] [Abstract][Full Text] [Related]  

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