BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

147 related articles for article (PubMed ID: 3426372)

  • 1. [Familial Miller-Dieker syndrome and (15;17) chromosome translocation].
    Goutières F; Aicardi J; Rethore MO; Prieur M; Lejeune J
    Arch Fr Pediatr; 1987; 44(7):501-4. PubMed ID: 3426372
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Apparent Smith-Lemli-Opitz syndrome and Miller-Dieker syndrome in a family with segregating translocation t(7;17)(q34;p13.1).
    Berry R; Wilson H; Robinson J; Sandlin C; Tyson W; Campbell J; Porreco R; Manchester D
    Am J Med Genet; 1989 Nov; 34(3):358-65. PubMed ID: 2596525
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Miller-Dieker syndrome due to maternal cryptic translocation t(10;17) (q26.3;p13.3).
    Masuno M; Imaizumi K; Nakamura M; Matsui K; Goto A; Kuroki Y
    Am J Med Genet; 1995 Dec; 59(4):441-3. PubMed ID: 8585563
    [TBL] [Abstract][Full Text] [Related]  

  • 4. DNA analysis in patients with lissencephaly type I and other cortical dysplasias.
    Oostra BA; de Rijk-van Andel JF; Eussen HJ; van Hemel JO; Halley DJ; Niermeijer MF
    Am J Med Genet; 1991 Sep; 40(3):383-6. PubMed ID: 1951447
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial Miller-Dieker syndrome associated with pericentric inversion of chromosome 17.
    Greenberg F; Stratton RF; Lockhart LH; Elder FF; Dobyns WB; Ledbetter DH
    Am J Med Genet; 1986 Apr; 23(4):853-9. PubMed ID: 3963054
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Miller-Dieker syndrome with der(17)t(12;17)(q24.33;p13.3)pat presenting with a potential risk of mis-identification as a de novo submicroscopic deletion of 17p13.3.
    Kim YJ; Byun SY; Jo SA; Shin YB; Cho EH; Lee EY; Hwang SH
    Korean J Lab Med; 2011 Jan; 31(1):49-53. PubMed ID: 21239872
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Miller-Dieker syndrome. Detection of a cryptic chromosome translocation using in situ hybridization in a family with multiple affected offspring.
    Alvarado M; Bass HN; Caldwell S; Jamehdor M; Miller AA; Jacob P
    Am J Dis Child; 1993 Dec; 147(12):1291-4. PubMed ID: 8249946
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Acute lymphoblastic leukemia in a patient with Miller-Dieker syndrome.
    Czuchlewski DR; Andrews J; Madden R; Clericuzio CL; Zhang QY
    J Pediatr Hematol Oncol; 2008 Nov; 30(11):865-8. PubMed ID: 18989166
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.
    Tüysüz B; Hacihanefioglu S; Silahtaroglu A; Yilmaz S; Deviren A; Cenani A
    Genet Couns; 2000; 11(4):355-61. PubMed ID: 11140413
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Partial duplication of 17 long arm.
    Lenzini E; Leszl A; Artifoni L; Casellato R; Tenconi R; Baccichetti C
    Ann Genet; 1988; 31(3):175-80. PubMed ID: 3265610
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A partial trisomy 15q due to 15;17 translocation detected by conventional cytogenetic and FISH techniques.
    Cora T; Acar H; Oran B
    Genet Couns; 2000; 11(1):25-32. PubMed ID: 10756424
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Unbalanced translocation (15;17)(q13;13.3) with apparent Prader-Willi syndrome but without Miller-Dieker syndrome.
    Elder FF; Nichols MM; Hood OJ; Harrison WR
    Am J Med Genet; 1985 Mar; 20(3):519-24. PubMed ID: 3993677
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Partial trisomy 4q and monosomy 9p resulting from a familial translocation t(4;9)(q27;p24) in a child with choanal atresia.
    Wouters CH; van Bodegom TM; Moll HA; Govaerts LC
    Ann Genet; 1999; 42(3):160-5. PubMed ID: 10526659
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Bilateral periventricular nodular heterotopia and lissencephaly in an infant with unbalanced t(12;17)(q24.31; p13.3) translocation.
    Grosso S; Fichera M; Galesi O; Luciano D; Pucci L; Giardini F; Berardi R; Balestri P
    Dev Med Child Neurol; 2008 Jun; 50(6):473-6. PubMed ID: 18384621
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [A case of Miller-Dieker syndrome associated with satellite on chromosome 17p].
    Obara Y; Koseki N; Fujiwara J; Kikuchi M; Miura T; Funato T; Kaku M
    Rinsho Byori; 2001 Feb; 49(2):189-92. PubMed ID: 11307315
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Miller-Dieker syndrome: a new case with cerebral echographic study].
    Vaquerizo-Madrid J; Gómez-Martín H; Rincón-Rodera P; Alonso-Luengo O
    Rev Neurol; 2000 Jan 1-15; 30(1):48-50. PubMed ID: 10742996
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Partial deletion of LIS1: a pitfall in molecular diagnosis of Miller-Dieker syndrome.
    Izumi K; Kuratsuji G; Ikeda K; Takahashi T; Kosaki K
    Pediatr Neurol; 2007 Apr; 36(4):258-60. PubMed ID: 17437911
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Two cases of deletion 5p syndrome: one with paternal involvement and another with atypical presentation.
    Azman BZ; Akhir SM; Zilfalil BA; Ankathil R
    Singapore Med J; 2008 Apr; 49(4):e98-e100. PubMed ID: 18418516
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Lissencephalia syndromes].
    Bode H; Bubl R
    Schweiz Rundsch Med Prax; 1992 Dec; 81(51):1529-33. PubMed ID: 1470795
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Risk of abnormal pregnancy outcome in carriers of balanced reciprocal translocations involving the Miller-Dieker syndrome (MDS) critical region in chromosome 17p13.3.
    Pollin TI; Dobyns WB; Crowe CA; Ledbetter DH; Bailey-Wilson JE; Smith AC
    Am J Med Genet; 1999 Aug; 85(4):369-75. PubMed ID: 10398263
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.