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 *

126 related articles for article (PubMed ID: 29485808)

  • 1. Distal 13q monosomy and neural tube defects.
    Lurie IW; Novikova IV; Tarletskaya OA; Lazarevich AA; Gromyko OA
    Genet Couns; 2016; 27(2):177-86. PubMed ID: 29485808
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Partial monosomy 13q (13q21.32--->qter) and partial trisomy 8p (8p1--->pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization.
    Chen CP; Su YN; Tsai FJ; Lin MH; Wu PC; Chern SR; Lee CC; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2011 Jun; 50(2):205-11. PubMed ID: 21791309
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Familial t(11;13)(q21;q14) and the duplication 11q, 13q phenotype.
    Park JP; McDermet MK; Doody AM; Marin-Padilla JM; Moeschler JB; Wurster-Hill DH
    Am J Med Genet; 1993 Jan; 45(1):46-8. PubMed ID: 8418658
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Chromosomal abnormalities in fetuses with open neural tube defects: prenatal identification with ultrasound.
    Sepulveda W; Corral E; Ayala C; Be C; Gutierrez J; Vasquez P
    Ultrasound Obstet Gynecol; 2004 Apr; 23(4):352-6. PubMed ID: 15065184
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Neural tube defects and the 13q deletion syndrome: evidence for a critical region in 13q33-34.
    Luo J; Balkin N; Stewart JF; Sarwark JF; Charrow J; Nye JS
    Am J Med Genet; 2000 Mar; 91(3):227-30. PubMed ID: 10756348
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal diagnosis of de novo partial trisomy 13q (13q22 --> qter) and partial monosomy 8p (8p23.3 --> pter) associated with holoprosencephaly, premaxillary agenesis, hexadactyly, and a hypoplastic left heart.
    Chen CP; Chern SR; Hsu CY; Lee CC; Lee MS; Wang W
    Prenat Diagn; 2005 Apr; 25(4):334-6. PubMed ID: 15849788
    [No Abstract]   [Full Text] [Related]  

  • 7. Clinical and cytogenetic features of a patient with partial trisomy 8q and partial monosomy 13q delineated by array comparative genomic hybridization.
    Sohn YB; Yun JN; Park SJ; Park MS; Kim SH; Lee JH
    Ann Clin Lab Sci; 2013; 43(3):332-6. PubMed ID: 23884231
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 3p partial trisomy and 13q partial monosomy with congenital malformations and psychomotor developmental delay.
    Rodovalho-Doriqui MJ; Freitas PL; Pinho JD; Cavalli LR; Pereira SR
    Genet Mol Res; 2013 Jul; 12(3):2562-6. PubMed ID: 23979887
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Chromosomal anomalies and additional sonographic findings in fetuses with open neural tube defects.
    Yazici LE; Malatyalioglu E; Sakinci M; Tosun M; Bildircin FD; Ogur G; Karayel M
    Arch Gynecol Obstet; 2012 Dec; 286(6):1393-8. PubMed ID: 22836815
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Evolution of prenatal detection of neural tube defects in the pregnant population of the city of Barcelona from 1992 to 2006.
    Salvador J; Arigita M; Carreras E; Lladonosa A; Borrell A
    Prenat Diagn; 2011 Dec; 31(12):1184-8. PubMed ID: 22025380
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mini-review: toward understanding mechanisms of genetic neural tube defects in mice.
    Harris MJ; Juriloff DM
    Teratology; 1999 Nov; 60(5):292-305. PubMed ID: 10525207
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis of the 13q-syndrome through three-dimensional ultrasonography: a case report.
    Araujo Júnior E; Filho HA; Pires CR; Filho SM
    Arch Gynecol Obstet; 2006 Jul; 274(4):243-5. PubMed ID: 16491370
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Etiology, pathogenesis and prevention of neural tube defects.
    Padmanabhan R
    Congenit Anom (Kyoto); 2006 Jun; 46(2):55-67. PubMed ID: 16732763
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Analysis on 2158 neural tube defects diagnosed prenatally by ultrasound examination].
    Wang Y; Liang J; Zhou G; Miao L; Zhu J; Wu Y
    Hua Xi Yi Ke Da Xue Xue Bao; 2000 Jun; 31(2):220-2. PubMed ID: 12515142
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosome.
    Lukusa T; van den Berghe L; Smeets E; Fryns JP
    Ann Genet; 1999; 42(4):215-20. PubMed ID: 10674161
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 13q Deletion and central nervous system anomalies: further insights from karyotype-phenotype analyses of 14 patients.
    Ballarati L; Rossi E; Bonati MT; Gimelli S; Maraschio P; Finelli P; Giglio S; Lapi E; Bedeschi MF; Guerneri S; Arrigo G; Patricelli MG; Mattina T; Guzzardi O; Pecile V; Police A; Scarano G; Larizza L; Zuffardi O; Giardino D
    J Med Genet; 2007 Jan; 44(1):e60. PubMed ID: 17209130
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Associated malformations in infants and fetuses with upper or lower neural tube defects.
    Kälién B; Robert E; Harris J
    Teratology; 1998 Feb; 57(2):56-63. PubMed ID: 9562677
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Exencephaly-anencephaly Sequence.
    ; Monteagudo A
    Am J Obstet Gynecol; 2020 Dec; 223(6):B5-B8. PubMed ID: 33168213
    [No Abstract]   [Full Text] [Related]  

  • 19. Prenatal diagnosis of partial monosomy 13q associated with occipital encephalocoele in a fetus.
    Chen CP; Liu FF; Jan SW; Wang KG; Lan CC
    Prenat Diagn; 1996 Jul; 16(7):664-6. PubMed ID: 8843478
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic heterogeneity in neural tube defects.
    Simpson JL; Mills J; Rhoads GG; Cunningham GC; Conley MR; Hoffman HJ
    Ann Genet; 1991; 34(3-4):279-86. PubMed ID: 1809238
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.