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 *

137 related articles for article (PubMed ID: 37731249)

  • 1. Molecular characterization of
    Ambulkar PS; Liehr T; Jain M; Waghmare J; Gangane N; Narang P; Pal AK
    J Genet; 2023; 102():. PubMed ID: 37731249
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A child with intellectual disability and dysmorphism due to complex ring chromosome 6: identification of molecular mechanism with review of literature.
    Sheth F; Liehr T; Shah V; Shah H; Tewari S; Solanki D; Trivedi S; Sheth J
    Ital J Pediatr; 2018 Oct; 44(1):114. PubMed ID: 30305128
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Smallest critical region for microcephaly in a patient with mosaic ring chromosome 13.
    Su PH; Chen CP; Su YN; Chen SJ; Lin LL; Chen JY
    Genet Mol Res; 2013 Apr; 12(2):1311-7. PubMed ID: 23661454
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical and molecular-cytogenetic studies in seven patients with ring chromosome 18.
    Stankiewicz P; Brozek I; Hélias-Rodzewicz Z; Wierzba J; Pilch J; Bocian E; Balcerska A; Wozniak A; Kardaś I; Wirth J; Mazurczak T; Limon J
    Am J Med Genet; 2001 Jul; 101(3):226-39. PubMed ID: 11424138
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An unexpected finding in a child with neurological problems: mosaic ring chromosome 18.
    Koç A; Kan D; Karaer K; Ergün MA; Karaoğuz MY; Gücüyener K; Hinreiner S; Liehr T; Perçin EF
    Eur J Pediatr; 2008 Jun; 167(6):655-9. PubMed ID: 17668239
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mosaic ring chromosome 14 and monosomy 14 presenting with growth retardation, epilepsy, and blepharophimosis.
    Hou JW
    Chang Gung Med J; 2004 May; 27(5):373-8. PubMed ID: 15366814
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Transmission of a ring chromosome 18 from a mother with 46,XX/47,XX, + r(18) mosaicism to her daughter, resulting in a 46,XX,r(18) karyotype.
    Jenderny J; Caliebe A; Beyer C; Grote W
    J Med Genet; 1993 Nov; 30(11):964-5. PubMed ID: 8301656
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Ring chromosome 16: a new case.
    Vianello MG; Cottafava F; Bartoli D; Franzone G; Casazzava R; Gastaldi R
    Ann Genet; 1990; 33(1):36-9. PubMed ID: 2195979
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Ring chromosome 15: characterization by array CGH.
    Glass IA; Rauen KA; Chen E; Parkes J; Alberston DG; Pinkel D; Cotter PD
    Hum Genet; 2006 Jan; 118(5):611-7. PubMed ID: 16267671
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Unbalanced translocation, t(18;21), detected by fluorescence in situ hybridization (FISH) in a child with 18q- syndrome and a ring chromosome 21.
    McGinniss MJ; Rosenberg C; Stetten G; Schinzel AA; Binkert F; Petersen MB; Kearns WG; Kazazian HH; Pearson PL; Antonarakis SE
    Am J Med Genet; 1993 Jul; 46(6):647-51. PubMed ID: 8362906
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mosaic r(13) resulting in large deletion of chromosome 13q in a newborn female with multiple congenital anomalies.
    Lorentz CP; Jalal SM; Thompson DM; Babovic-Vuksanovic D
    Am J Med Genet; 2002 Jul; 111(1):61-7. PubMed ID: 12124737
    [TBL] [Abstract][Full Text] [Related]  

  • 12. De novo mosaic ring chromosome 18 in a child with mental retardation, epilepsy and immunological problems.
    Lo-Castro A; El-Malhany N; Galasso C; Verrotti A; Nardone AM; Postorivo D; Palmieri C; Curatolo P
    Eur J Med Genet; 2011; 54(3):329-32. PubMed ID: 21333764
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Tetrasomy 21 pter→q21.3 due to an extra +dic(21;21)mat in a severely psychomotor-retarded female patient without Down syndrome phenotype.
    Takano T; Nakabayashi K; Ota H; Arai Y; Kamura H; Hata K
    Eur J Med Genet; 2020 Apr; 63(4):103824. PubMed ID: 31830537
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Atypical Down syndrome phenotype in a girl with 21;21 translocation trisomy.
    Tuysuz B; Yavuz A; Ozdil M; Caferler J; Ozon H
    Genet Couns; 2010; 21(1):61-7. PubMed ID: 20420031
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Array-CGH characterization and genotype-phenotype analysis in a patient with a ring chromosome 6.
    Ciocca L; Surace C; Digilio MC; Roberti MC; Sirleto P; Lombardo A; Russo S; Brizi V; Grotta S; Cini C; Angioni A
    BMC Med Genomics; 2013 Feb; 6():3. PubMed ID: 23398904
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Ring 21 chromosome and a satellited 1p in the same patient: novel origin for an ectopic NOR.
    Ki A; Rauen KA; Black LD; Kostiner DR; Sandberg PL; Pinkel D; Albertson DG; Norton ME; Cotter PD
    Am J Med Genet A; 2003 Jul; 120A(3):365-9. PubMed ID: 12838556
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mosaic chromosome 18 anomaly delineated in a child with dysmorphism using a three-pronged cytogenetic techniques approach: a case report.
    Sheth H; Trivedi S; Liehr T; Patel K; Jain D; Sheth J; Sheth F
    BMC Med Genomics; 2020 Sep; 13(1):141. PubMed ID: 32972420
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis of mosaic ring chromosome 22 associated with cardiovascular abnormalities and intrauterine growth restriction.
    Chen CP; Chern SR; Chang TY; Lee CC; Chen LF; Tzen CY; Wang W; Lin CJ; Yang BP; Yang LS
    Prenat Diagn; 2003 Jan; 23(1):40-3. PubMed ID: 12533811
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4.
    Chen CP; Chen M; Su YN; Tsai FJ; Chern SR; Wu PC; Chen WL; Chen LF; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2011 Jun; 50(2):188-95. PubMed ID: 21791306
    [TBL] [Abstract][Full Text] [Related]  

  • 20. De novo ring chromosome 6 in a child with multiple congenital anomalies.
    Ahzad HA; Ramli SF; Loong TM; Salahshourifar I; Zilfalil BA; Yusoff NM
    Kobe J Med Sci; 2010 Sep; 56(2):E79-84. PubMed ID: 21063149
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.