BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

112 related articles for article (PubMed ID: 8835329)

  • 1. De novo balanced 5;21 translocation in a child with acrobrachycephaly, ventriculomegaly, pulmonary stenosis, ectopic anus and mental retardation.
    Hordnes K; Engebretsen LF; Knudtzon J
    Clin Genet; 1995 Dec; 48(6):321-3. PubMed ID: 8835329
    [TBL] [Abstract][Full Text] [Related]  

  • 2. De novo reciprocal 1p;2q translocation in a child with multiple congenital anomalies/mental retardation syndrome.
    Chitayat D; Fagerstrom CL; Kalousek DK; Rootman J; Taylor GP; Hall JG
    Am J Med Genet; 1989 Jan; 32(1):36-41. PubMed ID: 2495721
    [TBL] [Abstract][Full Text] [Related]  

  • 3. De novo t(X;21)(q28;q11) in a girl with phenotypic features of Williams-Beuren syndrome.
    Telvi L; Pinard JM; Ion R; Sinet PM; Nicole A; Feingold J; Dulac O; Pompidou A; Ponsot G
    J Med Genet; 1992 Oct; 29(10):747-9. PubMed ID: 1433240
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cohen syndrome and de novo reciprocal translocation t(5;7)(q33.1;p15.1).
    Fryns JP; Kleczkowska A; Smeets E; Thiry P; Geutjens J; Van den Berghe H
    Am J Med Genet; 1990 Dec; 37(4):546-7. PubMed ID: 2260606
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Asplenia syndrome in a child with a balanced reciprocal translocation of chromosomes 11 and 20 [46,XX,t(11;20)(q13.1;q13.13)].
    Freeman SB; Muralidharan K; Pettay D; Blackston RD; May KM
    Am J Med Genet; 1996 Feb; 61(4):340-4. PubMed ID: 8834045
    [TBL] [Abstract][Full Text] [Related]  

  • 6. De novo balanced translocation (2;10)(q24;q22) associated with mental retardation.
    Santos CB; Discepoli G; Pigliapoco F; Boy R; Pimentel MM
    Ann Genet; 2003; 46(4):471-3. PubMed ID: 14659784
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Wilms' tumor, malformative syndrome, mental retardation and de novo constitutional translocation, t(7;13)(q36;q13).
    Bernard JL; Baeteman MA; Mattei JF; Raybaud C; Giraud F
    Eur J Pediatr; 1984 Jan; 141(3):175-7. PubMed ID: 6321191
    [TBL] [Abstract][Full Text] [Related]  

  • 8. De novo double translocation 3;13 and 4;8;18 in a patient with mental retardation and skeletal abnormalities.
    Battisti C; Bonaglia MC; Giglio S; Anichini C; Pucci L; Dotti MT; Zuffardi O; Federico A
    Am J Med Genet A; 2003 Mar; 117A(3):207-11. PubMed ID: 12599183
    [TBL] [Abstract][Full Text] [Related]  

  • 9. De novo 3q/7q translocation and associated interstitial 7q35 deletion.
    Fryns JP; Kleczkowska A; van den Berghe H
    Clin Genet; 1988 Jan; 33(1):60-2. PubMed ID: 3342549
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Opitz trigonocephaly C syndrome in a boy with a de novo balanced reciprocal translocation t(3;18)(q13.13;q12.1).
    Chinen Y; Kaname T; Yanagi K; Saito N; Naritomi K; Ohta T
    Am J Med Genet A; 2006 Aug; 140(15):1655-7. PubMed ID: 16835930
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Double chromosome anomaly: interstitial deletion 5q and reciprocal translocation (1;11)(p22;q21).
    de Michelena MI; Villacorta J; Chávez J
    Am J Med Genet; 1990 May; 36(1):29-32. PubMed ID: 2185634
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mental retardation with 45 chromosomes 45,XX,--5,--14,+der(5) t(5,14)(p15;q13) mat due to familial balanced reciprocal translocation.
    Fried K; Tieder M; Beer S; Rosenblatt M; Krespin HI
    J Med Genet; 1977 Feb; 14(1):68-72. PubMed ID: 839506
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Unusual chromosomal mosaicism as a cause of mental retardation and congenital malformations in a familial reciprocal translocation carrier, t(17;22)(q24.2;q11.23).
    Dufke A; Mayrhofer H; Enders H; Kaiser P; Leipoldt M
    Cytogenet Cell Genet; 2001; 93(3-4):168-70. PubMed ID: 11528107
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A case of 46,XY,t(1;13) (q24;q32) with mental retardation.
    Wilbur L; Curcuru-Giordano FM; Krishna SG; Kardon NB; Jenkins EC
    Hum Genet; 1977 Jun; 37(2):239-42. PubMed ID: 885541
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An intellectually disabled patient with the 5q14.3q15 microdeletion syndrome associated with an apparently de novo t(2;5)(q13;q14).
    Toral-López J; Buentello-Volante B; Balderas-Minor MM; Amezcua-Herrera C; Valdes-Miranda JM; González-Huerta LM; Gudiño M; Cuevas-Covarrubias SA; Zenteno JC
    Am J Med Genet A; 2012 Apr; 158A(4):942-6. PubMed ID: 22419405
    [No Abstract]   [Full Text] [Related]  

  • 16. De novo pericentric inversion of chromosome 5 in a girl with mental retardation and unilateral ear malformation.
    Ulucan H; Akin R; Kösem M; Gül D
    Am J Med Genet A; 2006 Feb; 140(3):298-9. PubMed ID: 16411238
    [No Abstract]   [Full Text] [Related]  

  • 17. Familial partial trisomy 5p resulting from segregation of an insertional translocation.
    Gustavson KH; Lundberg PO; Nicol P
    Clin Genet; 1988 Jun; 33(6):404-9. PubMed ID: 3168312
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A child with multiple congenital anomalies due to partial trisomy 7q22.1 → qter resulting from a maternally inherited balanced translocation: a case report and review of literature.
    Paththinige CS; Sirisena ND; Kariyawasam UGIU; Ediriweera RC; Kruszka P; Muenke M; Dissanayake VHW
    BMC Med Genomics; 2018 May; 11(1):44. PubMed ID: 29739404
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Tertiary trisomy 14q--, due to paternal balanced translocation 46,XY,t(1;14)(q44;q22).
    Kovacs G; Mihai C
    Hum Genet; 1979 Jun; 49(2):175-8. PubMed ID: 468247
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A 5q12.1-5q12.3 microdeletion in a case with a balanced exceptional complex chromosomal rearrangement.
    Cetin Z; Yakut S; Clark OA; Mihci E; Berker S; Luleci G
    Gene; 2013 Mar; 516(1):176-80. PubMed ID: 23262338
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.