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 *

151 related articles for article (PubMed ID: 11857553)

  • 1. Craniofacial anomalies, deafness, brachydactyly, short stature, and moderate mental retardation due to a cryptic 6p;11q translocation.
    Mégarbané A; Bejjani BA; Shaffer LG; Jambart S; Souraty N; Kashork CD; Le Merrer M
    Am J Med Genet; 2002 Feb; 108(1):69-74. PubMed ID: 11857553
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Partial trisomy 6p from a de novo translocation (6;18) with variable mosaicism in different tissues.
    Rudnik-Schöneborn S; Schubert R; Majewski F; Haverkamp F; Schwanitz G
    Clin Genet; 1997 Aug; 52(2):126-9. PubMed ID: 9298749
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
    Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
    Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 6p subtelomere deletion with congenital glaucoma, severe mental retardation, and growth impairment.
    Nakane T; Kousuke N; Sonoko H; Yuko K; Sato H; Kubota T; Sugita K
    Pediatr Int; 2013 Jun; 55(3):376-81. PubMed ID: 23782370
    [TBL] [Abstract][Full Text] [Related]  

  • 5. De novo complex chromosome rearrangement in identical twins with multiple congenital anomalies.
    Wakita Y; Narahara K; Tsuji K; Yokoyama Y; Ninomiya S; Murakami R; Kikkawa K; Seino Y
    Hum Genet; 1992 Mar; 88(5):596-8. PubMed ID: 1551663
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Monozygotic twins discordant for partial trisomy 1.
    Watson WJ; Katz VL; Albright SG; Rao KW; Aylsworth AS
    Obstet Gynecol; 1990 Nov; 76(5 Pt 2):949-51. PubMed ID: 2216262
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Detection of a cryptic translocation t(13;20)(q34;p13) in an unexplained case of MCA/MR: value of FISH over high resolution banding.
    de Die-Smulders CE; Engelen JJ; Albrechts JC; Hamers GJ
    Am J Med Genet; 1999 Oct; 86(4):385-8. PubMed ID: 10494096
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Caudal appendage, short terminal phalanges, deafness, cryptorchidism and mental retardation: a new syndrome?
    Lynch SA; Lee SG; Murday VA
    Clin Dysmorphol; 1994 Oct; 3(4):340-6. PubMed ID: 7894739
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Marker chromosomes as a product of familial translocation (11;22) identified with molecular cytogenetic methods].
    Stankiewicz P; Korniszewski L; Bocian E; Stańczak H
    Pediatr Pol; 1996 Mar; 71(3):241-5. PubMed ID: 8966096
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Subtelomeric deletions of chromosome 6p: molecular and cytogenetic characterization of three new cases with phenotypic overlap with Ritscher-Schinzel (3C) syndrome.
    Descipio C; Schneider L; Young TL; Wasserman N; Yaeger D; Lu F; Wheeler PG; Williams MS; Bason L; Jukofsky L; Menon A; Geschwindt R; Chudley AE; Saraiva J; Schinzel AA; Guichet A; Dobyns WE; Toutain A; Spinner NB; Krantz ID
    Am J Med Genet A; 2005 Apr; 134A(1):3-11. PubMed ID: 15704124
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Precocious puberty associated with partial trisomy 18q and monosomy 11q.
    Mutesa L; Hellin AC; Jamar M; Pierquin G; Bours V; Verloes A
    Genet Couns; 2007; 18(2):201-7. PubMed ID: 17710872
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Partial monosomy of 7q32 in a case of de novo rcp(7;15)(q32;q15).
    D'Alessandro E; Ligas C; Lo Re ML; Marcanio MP; Gentile T; Del Porto G
    J Med Genet; 1994 May; 31(5):413-5. PubMed ID: 8064823
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Submicroscopic unbalanced translocation resulting in del10p/dup13q detected by subtelomere FISH.
    Roos A; Rudnik-Schöneborn S; Eggermann K; Eggermann T; Senderek J; Schwanitz G; Zerres K; Schüler HM
    Eur J Med Genet; 2006; 49(6):505-10. PubMed ID: 16905374
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Partial trisomy 4(q31qter) due to maternal 4;5 balanced translocation in a neonate.
    Senses DA; Silan F; Uzun H; Alagöz D; Zafer C; Kocabay K; Karaüzüm SB; Cetin Z
    Genet Couns; 2007; 18(2):163-70. PubMed ID: 17710868
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A case of severe mental and developmental retardation associated with 14q terminal monosomy/5q terminal trisomy.
    Hirayama T
    J Nippon Med Sch; 2010 Feb; 77(1):40-4. PubMed ID: 20154457
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Dubowitz syndrome and atopic eczema. Case report of monozygotic twins].
    Möhrenschlager M; Beham A; Albrecht J; Abeck D; Ring J
    Hautarzt; 2000 Feb; 51(2):95-100. PubMed ID: 10743581
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [The phenotype of the trisomy of the short arm of chromosome no. 4. (a new case with t (4p; 11q) (author's transl)].
    Kessel E; Pfeiffer RA; Kosenow W
    Klin Padiatr; 1976 May; 188(3):215-9. PubMed ID: 945417
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Trisomy 18 in monozygotic twins with discordant phenotypes.
    Lee JT; Chou HC; Tsao PN; Hsieh WS; Hwu WL
    J Formos Med Assoc; 2004 Apr; 103(4):314-6. PubMed ID: 15175830
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Partial trisomy 8p (8p11.2-->pTER) and deletion of 13q (13q32-->qTER): case report.
    Yeşilyurt A; Dilli D; Oguz S; Dilmen U; Altug N; Candemir Z
    Genet Couns; 2011; 22(1):35-40. PubMed ID: 21614986
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of a subtle chromosomal translocation in a family with recurrent miscarriages and a child with multiple congenital anomalies. A case report.
    Shaffer LG; Spikes AS; Macha M; Dunn R
    J Reprod Med; 1996 May; 41(5):367-71. PubMed ID: 8725766
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.