BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 9128937)

  • 1. Two sibs with partial trisomy 2q.
    Barnicoat AJ; Abusaad I; Mackie CM; Robards MF
    Am J Med Genet; 1997 May; 70(2):166-70. PubMed ID: 9128937
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mild dysmorphic signs in two male sibs with partial trisomy 2q32.1-->q35 due to maternal ins(14;2) translocation.
    Lukusa T; Devriendt K; Jaeken J; Fryns JP
    Clin Dysmorphol; 1999 Jan; 8(1):47-51. PubMed ID: 10327251
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Partial 4q trisomy. Apropos of 3 cases].
    Dutrillaux B; Laurent C; Forabosco A; Noel B; Suerinc E; Biemont MC; Cotton JB
    Ann Genet; 1975 Mar; 18(1):21-7. PubMed ID: 238457
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A patient with partial duplication 2q and partial deficiency 11q.
    Ho CK; Henderson KC; Bowyer FP; Eilers KB; Andrews LG
    Am J Med Genet; 1987 Nov; 28(3):575-9. PubMed ID: 3322008
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Trisomy 2q35-q37 due to insertion of 2q material into 17q25: clinical, cytogenetic, and molecular cytogenetic characterization.
    Fritz B; Müller-Navia J; Hillig U; Köhler M; Aslan M; Rehder H
    Am J Med Genet; 1999 Dec; 87(4):297-301. PubMed ID: 10588833
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Complete trisomy 9. Two additional cases.
    Delicado A; Iñiguez L; Lopez Pajares I; Omeñaca F
    Ann Genet; 1985; 28(1):63-6. PubMed ID: 3874593
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 2q35qter duplication syndrome: phenotypic definition.
    Grammatico P; Di Rosa C; Rinaldi R; Roccella M; Cupilari F; Sbezzi T; Del Porto G
    Genet Couns; 1997; 8(4):327-34. PubMed ID: 9457503
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Joubert syndrome co-existing with partial Xp trisomy: review of the literature.
    Güven GS; Fenerci EY; Deviren A; Ozkiliç A; Yüksel A; Hacihanefioğlu S
    Genet Couns; 2004; 15(3):321-8. PubMed ID: 15517825
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Partial trisomy 17p12pter, associated with pre and postnatal growth retardation, dysmorphic facial and digital features, developmental delay, and signs of HMSN1 in early childhood.
    Vogt J; Hill S; Brueton L
    Eur J Med Genet; 2006; 49(5):439-43. PubMed ID: 16488202
    [No Abstract]   [Full Text] [Related]  

  • 10. Trisomy 7p: report of 2 patients and literature review.
    Arens YH; Toutain A; Engelen JJ; Offermans JP; Hamers AJ; Schrander JJ; Pulles-Heintzberger CF; Schrander-Stumpel CT
    Genet Couns; 2000; 11(4):347-54. PubMed ID: 11140412
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Partial trisomy and monosomy for short arm of chromosome number 5 in two sibs and a balanced translocation carrier father.
    Kulkarni MV; Patel ZM; Peter JJ; Ambani LM
    Indian Pediatr; 1981 Apr; 18(4):263-6. PubMed ID: 7287154
    [No Abstract]   [Full Text] [Related]  

  • 12. Trisomy of 8q22.3 approximately q23-qter following an unbalanced 1;8 translocation in a boy with multiple anomalies.
    Ergun MA; Balci S; Konaç E; Kan D; Menevşe S; Bartsch O
    Turk J Pediatr; 2004; 46(4):384-7. PubMed ID: 15641279
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Partial trisomy 11q 46, XX, 4q+ by translocation t (4; 11) (q35; q12)].
    Le Chevalier C; Chabrolle JP; Rossier A
    Ann Pediatr (Paris); 1978 Nov; 25(9):501-4, 507. PubMed ID: 16114368
    [No Abstract]   [Full Text] [Related]  

  • 14. Duplication of (2)(q11.1-q13.2) in a boy with mental retardation and cleft lip and palate: another clefting gene locus on proximal 2q?
    Riegel M; Schinzel A
    Am J Med Genet; 2002 Jul; 111(1):76-80. PubMed ID: 12124740
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Trisomy 16p: a longitudinal profile and photo essay.
    Sommer A; Pastore M; Wenger G
    Am J Med Genet A; 2006 Jan; 140(2):174-9. PubMed ID: 16353251
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Trisomy for the distal segment of the short arm of chromosome 17 in a boy with mild mental retardation and some dysmorphic features.
    Mégarbané A; Souraty N; Theophile D; Vekemans M; Samaras L; Ghorayeb Z
    Ann Genet; 1997; 40(1):55-9. PubMed ID: 9150851
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Partial trisomy 15q: report of a patient and literature review.
    Chandler K; Schrander-Stumpel CT; Engelen J; Theunissen P; Fryns JP
    Genet Couns; 1997; 8(2):91-7. PubMed ID: 9219006
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A rec(4) dup 4p inherited from a maternal inv(4)(p15q35): case report and review.
    Garcia-Heras J; Martin J
    Am J Med Genet; 2002 May; 109(3):226-30. PubMed ID: 11977183
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pure partial trisomy of 6p12.1-p22.1 secondary to a familial 12/6 insertion in two malformed babies.
    Fogu G; Bandiera P; Cambosu F; Carta AR; Pilo L; Serra G; Soro G; Tondi M; Tusacciu G; Montella A
    Eur J Med Genet; 2007; 50(2):103-11. PubMed ID: 17185054
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Recombinant 4 syndrome due to an unbalanced pericentric inversion of chromosome 4.
    Battaglia A; Brothman AR; Carey JC
    Am J Med Genet; 2002 Sep; 112(1):103-6. PubMed ID: 12239731
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.