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 *

128 related articles for article (PubMed ID: 14699616)

  • 1. Partial duplication 2p as the sole abnormality in two cases with anencephaly.
    Thangavelu M; Frolich G; Rogers D
    Am J Med Genet A; 2004 Jan; 124A(2):170-2. PubMed ID: 14699616
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Trisomy 2p syndrome: a fetus with anencephaly and postaxial polydactyly.
    Hahm GK; Barth RF; Schauer GM; Reiss R; Opitz JM
    Am J Med Genet; 1999 Nov; 87(1):45-8. PubMed ID: 10528246
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular cytogenetic characterization of a duplication of 15q24.2-q26.2 associated with anencephaly and neural tube defect.
    Chen CP; Chen CY; Chern SR; Wu PS; Chen SW; Lai ST; Lee CC; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2017 Aug; 56(4):550-553. PubMed ID: 28805617
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The value of chromosome analysis in cases of neural tube defects: a case of anencephaly associated with fetal dup(2)(p24----pter).
    Singer N; Gersen S; Warburton D
    Prenat Diagn; 1987 Oct; 7(8):567-71. PubMed ID: 3317387
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatal Diagnosis of Trisomy 2p due to Terminal 2p Duplication including Interstitial Telomeric Sequences.
    Marlet L; Alix E; Till M; Raskin-Champion F; Attia J; Boggio D; Sanlaville D; Schluth-Bolard C
    Cytogenet Genome Res; 2017; 153(3):117-124. PubMed ID: 29268249
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical picture: Multicolour karyotyping.
    Lee C; Murray MF; Miron PM; Marsden D; Irons M; Wilkins-Haug LE; Morton CC
    Lancet; 2001 Apr; 357(9264):1240. PubMed ID: 11458963
    [No Abstract]   [Full Text] [Related]  

  • 7. Regarding trisomy 2p syndrome.
    Wellesley D; Boyle T
    Am J Med Genet; 2000 Jun; 92(4):295. PubMed ID: 10842300
    [No Abstract]   [Full Text] [Related]  

  • 8. Unrelated patients with a rearrangement of chromosome 2 causing duplication of 2p23 and deletion of 2q37.
    Armstrong L; Allanson JE; Weaver DD; Bevan CJ; Hobart HH
    Am J Med Genet A; 2005 Apr; 134(3):299-304. PubMed ID: 15742366
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Minute chromosomal rearrangements detected prenatally by fluorescence in situ hybridization.
    Suzumori K; Tanemura M; Oya N; Suzumori N; Kim KC; Ohashi H; Fukushima Y
    Prenat Diagn; 1998 Jul; 18(7):725-30. PubMed ID: 9706655
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Duplication of 2q31-qter as a sole aberration in a case of non-Hodgkin's lymphoma.
    Bajalica-Lagercrantz S; Tingaard Pedersen N; Sørensen AG; Nordenskjöld M
    Cancer Genet Cytogenet; 1996 Sep; 90(2):102-5. PubMed ID: 8830716
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Ring chromosome 13: lack of distinct syndromes based on different breakpoints on 13q.
    Brandt CA; Hertz JM; Petersen MB; Vogel F; Noer H; Mikkelsen M
    J Med Genet; 1992 Oct; 29(10):704-8. PubMed ID: 1433229
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Cytogenetic and molecular characterization of a partial trisomy 2p arising from inverted duplication of 2p with terminal deletion of 2pter.
    Tirado CA; Henderson S; Uddin N; Stewart E; Iyer S; Ratner IM; Matthews E; Doolittle J; Garcia R; Valdez F; Dallaire S; Appleberry T; Payne D; Collins R
    Am J Med Genet A; 2009 Nov; 149A(11):2507-12. PubMed ID: 19876903
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal detection of de novo inversion of chromosome 9 with duplicated heterochromatic region and postnatal follow-up.
    Kim JJ; Rhee HS; Chung YT; Park SY; Choi SK
    Exp Mol Med; 1999 Sep; 31(3):134-6. PubMed ID: 10551261
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A de novo complex chromosomal rearrangement involving chromosomes 2, 3, and 10 associated with microcephaly and early onset spasticity.
    Emberger W; Petek E; Plecko-Starting B; Kroisel PM; Zierler H; Wagner K
    J Med Genet; 2000 Nov; 37(11):892-6. PubMed ID: 11185078
    [No Abstract]   [Full Text] [Related]  

  • 16. [Parental chromosome aberrations as a cause of anencephaly].
    Weise W
    Zentralbl Gynakol; 1974 Sep; 96(39):1227-30. PubMed ID: 4450829
    [No Abstract]   [Full Text] [Related]  

  • 17. Abnormal muscle development of the diaphragm in a fetus with 2p14-p16 duplication.
    Guilherme R; Guimiot F; Tabet AC; Khung-Savatovsky S; Gauthier E; Nouchy M; Benzacken B; Verloes A; Oury JF; Delezoide AL; Aboura A
    Am J Med Genet A; 2009 Dec; 149A(12):2892-7. PubMed ID: 19938079
    [No Abstract]   [Full Text] [Related]  

  • 18. Delimitation of duplicated segments and identification of their parental origin in two partial chromosome 3p duplications.
    Antonini S; Kim CA; Sugayama SM; Vianna-Morgante AM
    Am J Med Genet; 2002 Nov; 113(2):144-50. PubMed ID: 12407704
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Sperm segregation patterns by fluorescence in situ hybridization studies of a 46,XY,t(2;6) heterozygote giving rise to a rare triploid product of conception with a 69,XXY,t(2;6)(p12;q24)der(6)t(2;6)(p12;q24)pat karyotype.
    Lim AS; Lim TH; Kee SK; Chieng R; Tay SK
    Am J Med Genet A; 2003 Mar; 117A(2):172-6. PubMed ID: 12567417
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis of partial trisomy 2q. Case report.
    Matos A; Nogueira A; Criado B; Pereira S; Castedo S; Montenegro N
    Prenat Diagn; 1997 Sep; 17(9):874-6. PubMed ID: 9316134
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.