BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

317 related articles for article (PubMed ID: 16719274)

  • 41. Duane syndrome associated with features of the cat-eye syndrome and mosaicism for a supernumerary chromosome probably derived from number 22.
    Kalpakian B; Choy AE; Sparkes RS; Schreck RR
    J Pediatr Ophthalmol Strabismus; 1988; 25(6):293-7. PubMed ID: 24879932
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Supernumerary chromosome marker Der(22)t(11;22) resulting from a maternal balanced translocation.
    Hou JW
    Chang Gung Med J; 2003 Jan; 26(1):48-52. PubMed ID: 12656309
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Cri du chat mosaicism: an unusual case of partial deletion and partial deletion/ duplication of the short arm of chromosome 5, leading to an unusual cri du chat phenotype.
    Murru D; Boccone L; Ristaldi MS; Nucaro AL
    Genet Couns; 2008; 19(4):381-6. PubMed ID: 19239081
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Further delineation of 7p trisomy. Case report and review of literature.
    Pallotta R; Dalprà L; Fusilli P; Zuffardi O
    Ann Genet; 1996; 39(3):152-8. PubMed ID: 8839888
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Trisomy 18/trisomy 13 mosaicism in an adult with profound mental retardation and multiple malformations.
    Wilson WG; Shires MA; Willson KA; Wyandt HE; Harris LM; Kelly TE
    Am J Med Genet; 1983 Sep; 16(1):131-6. PubMed ID: 6638063
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [The (18)(q 22----qter) deletion in patients with complete clinical features of the De Grouchy syndrome].
    Vranjesević D; Dukić S; Jović N; Branković S; Kosanović M
    Neurol Croat; 1991; 40(1):39-47. PubMed ID: 2070033
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Cryptic mosaicism for monosomy 20 identified in renal tract cells.
    Stefanou EG; Crocker M; Boon A; Stewart H
    Clin Genet; 2006 Sep; 70(3):228-32. PubMed ID: 16922725
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Mosaic trisomy 21/monosomy 21 in a living female infant.
    Nguyen HP; Riess A; Krüger M; Bauer P; Singer S; Schneider M; Enders H; Dufke A
    Cytogenet Genome Res; 2009; 125(1):26-32. PubMed ID: 19617693
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Trisomy 14 mosaicism in a 5-year-old boy.
    Vachvanichsanong P; Jinorose U; Sangnuachua P
    Am J Med Genet; 1991 Jul; 40(1):80-3. PubMed ID: 1887854
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Lethal Pallister-Killian syndrome: phenotypic similarity with Fryns syndrome.
    Rodríguez JI; Garcia I; Alvarez J; Delicado A; Palacios J
    Am J Med Genet; 1994 Nov; 53(2):176-81. PubMed ID: 7856644
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Mosaic trisomy 14 with hepatic involvement.
    Iglesias A; McCurdy LD; Glass IA; Cotter PD; Illueca M; Perenyi A; Sansaricq C
    Ann Genet; 1997; 40(2):104-8. PubMed ID: 9259957
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
    Kolialexi A; Kitsiou S; Fryssira H; Sofocleous C; Kouvidi E; Tsangaris GT; Salavoura K; Mavrou A
    In Vivo; 2006; 20(4):473-8. PubMed ID: 16900777
    [TBL] [Abstract][Full Text] [Related]  

  • 53. An interstitial deletion of 7.1Mb in chromosome band 6p22.3 associated with developmental delay and dysmorphic features including heart defects, short neck, and eye abnormalities.
    Bremer A; Schoumans J; Nordenskjöld M; Anderlid BM; Giacobini M
    Eur J Med Genet; 2009; 52(5):358-62. PubMed ID: 19576304
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Lethal presentation of mosaic tetrasomy 12p (Pallister-Killian) syndrome.
    Young ID; Duckett DP; O'Reilly KM
    Ann Genet; 1989; 32(1):62-4. PubMed ID: 2751252
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Unilateral microtia in an infant with trisomy 18 mosaicism.
    Giannatou E; Leze H; Katana A; Kolialexi A; Mavrou A; Kanavakis E; Kitsiou-Tzeli S
    Genet Couns; 2009; 20(2):181-7. PubMed ID: 19650416
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Terminal 6q25.3 deletion and abnormal behaviour.
    Lukusa T; Willekens D; Lukusa N; De Cock F; Fryns JP
    Genet Couns; 2001; 12(3):213-21. PubMed ID: 11693783
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Trisomy 8: an international study of 70 patients.
    Riccardi VM
    Birth Defects Orig Artic Ser; 1977; 13(3C):171-84. PubMed ID: 890109
    [TBL] [Abstract][Full Text] [Related]  

  • 58. New case of non-mosaic tetrasomy 9p in a severely polymalformed newborn girl.
    de Azevedo Moreira LM; Freitas LM; Gusmão FA; Riegel M
    Birth Defects Res A Clin Mol Teratol; 2003 Dec; 67(12):985-8. PubMed ID: 14745919
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Pure familial 6q21q22.1 duplication in two generations.
    Pazooki M; Lebbar A; Roubergues A; Baverel F; Letessier D; Dupont JM
    Eur J Med Genet; 2007; 50(1):60-5. PubMed ID: 17071147
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Identification, characterization and clinical implications of two markers detected at prenatal diagnosis.
    Leite RP; Souto M; Carvalho B; Martins M; Chaves R; Morais A; Guedes-Pinto H; Wienberg J; Ribeiro E
    Prenat Diagn; 2006 Oct; 26(10):920-4. PubMed ID: 16845683
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.