BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

183 related articles for article (PubMed ID: 27644460)

  • 1. Miller-Dieker Syndrome with unbalanced translocation 45, X, psu dic(17;Y)(p13;p11.32) detected by fluorescence in situ hybridization and G-banding analysis using high resolution banding technique.
    Mishima T; Watari M; Iwaki Y; Nagai T; Kawamata-Nakamura M; Kobayashi Y; Fujieda S; Oikawa M; Takahashi N; Keira M; Yoshida H; Tonoki H
    Congenit Anom (Kyoto); 2017 Mar; 57(2):61-63. PubMed ID: 27644460
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. [Prenatal genetic analysis of two fetuses with Miller-Dieker syndrome].
    Lin S; Luo Y; Wu J; Chen B; Ji Y; Zhou Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb; 34(1):89-92. PubMed ID: 28186603
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Chromosome 17p13.3 deletion syndrome: aCGH characterization, prenatal findings and diagnosis, and literature review.
    Chen CP; Chang TY; Guo WY; Wu PC; Wang LK; Chern SR; Wu PS; Su JW; Chen YT; Chen LF; Wang W
    Gene; 2013 Dec; 532(1):152-9. PubMed ID: 24055730
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A new 17p13.3 microduplication including the PAFAH1B1 and YWHAE genes resulting from an unbalanced X;17 translocation.
    Hyon C; Marlin S; Chantot-Bastaraud S; Mabboux P; Beaujard MP; Al Ageeli E; Vazquez MP; Picard A; Siffroi JP; Portnoï MF
    Eur J Med Genet; 2011; 54(3):287-91. PubMed ID: 21195811
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Rare Concurrence of Two Congenital Disorders: Miller-Dieker Syndrome and T-Cell Lymphopenia.
    Chee SY; Guo JW; Huang CJ; Chien YH; Lee YC; Feng WK
    Cytogenet Genome Res; 2019; 157(4):227-230. PubMed ID: 31030199
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Neuronal migration genes and a familial translocation t (3;17): candidate genes implicated in the phenotype.
    Hadj Amor M; Dimassi S; Taj A; Slimani W; Hannachi H; Mlika A; Ben Helel K; Saad A; Mougou-Zerelli S
    BMC Med Genet; 2020 Feb; 21(1):26. PubMed ID: 32028920
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Miller-Dieker Syndrome due to a 5.5-Mb 17p Deletion in a 17;Y Pseudodicentric Chromosome.
    Bellucco FT; Nunes N; Colovati MES; Malinverni ACM; Caneloi TP; Soares MF; A Perez AB; Melaragno MI
    Cytogenet Genome Res; 2017; 152(1):29-32. PubMed ID: 28738335
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Prenatal diagnosis of a fetus with Miller-Dieker syndrome].
    Xu L; Huang H; Wang Y; An G; Lin N; Zhang M; Wu X; He D; Chen M; Lin Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Dec; 34(6):879-883. PubMed ID: 29188621
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Ventriculomegaly, intrauterine growth restriction, and congenital heart defects as salient prenatal sonographic findings of Miller-Dieker lissencephaly syndrome associated with monosomy 17p (17p13.2 --> pter) in a fetus.
    Chen CP; Liu YP; Lin SP; Chen M; Tsai FJ; Chen YT; Chen LF; Hwang JK; Wang W
    Taiwan J Obstet Gynecol; 2010 Mar; 49(1):81-6. PubMed ID: 20466299
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal diagnosis of monosomy 17p (17p13.3-->pter) associated with polyhydramnios, intrauterine growth restriction, ventriculomegaly, and Miller-Dieker lissencephaly syndrome in a fetus.
    Lin CY; Chen CP; Liau CL; Su PH; Tsao TF; Chang TY; Wang W
    Taiwan J Obstet Gynecol; 2009 Dec; 48(4):408-11. PubMed ID: 20045764
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Prenatal diagnosis of a fetus with Miller-Dieker syndrome].
    Zhang H; Yang X; Tang X; Li G; Tang D; Huang Z
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Nov; 37(11):1280-1282. PubMed ID: 33179240
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genomic copy number variations at 17p13.3 and epileptogenesis.
    Shimojima K; Sugiura C; Takahashi H; Ikegami M; Takahashi Y; Ohno K; Matsuo M; Saito K; Yamamoto T
    Epilepsy Res; 2010 May; 89(2-3):303-9. PubMed ID: 20227246
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridization.
    Kuwano A; Ledbetter SA; Dobyns WB; Emanuel BS; Ledbetter DH
    Am J Hum Genet; 1991 Oct; 49(4):707-14. PubMed ID: 1897521
    [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. Lissencephaly with der(17)t(17;20)(p13.3;p12.2)mat.
    Thomas MA; Duncan AM; Bardin C; Kaloustian VM
    Am J Med Genet A; 2004 Jan; 124A(3):292-5. PubMed ID: 14708103
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Prenatal diagnosis and genetic analysis of a fetus with Miller-Dieker syndrome].
    Duan F; Kong X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Jan; 38(1):71-73. PubMed ID: 33423263
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Array comparative genomic hybridization characterization of a 3.3-Mb 17p13.3-p13.2 deletion encompassing YWHAE, CRK, HIC1 and PAFAH1B1 in an 8-year-old girl with Miller-Dieker lissencephaly syndrome, congenital heart defects, growth restriction and developmental delay.
    Chen CP; Chang SY; Lin SP; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Chen WL; Wang W
    Taiwan J Obstet Gynecol; 2018 Oct; 57(5):765-768. PubMed ID: 30342670
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.