BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 2268978)

  • 1. "Isolated" radial ray defect may be due to Rothmund-Thomson syndrome.
    Moss C; Bacon CJ; Mueller RF
    Clin Genet; 1990 Oct; 38(4):318-9. PubMed ID: 2268978
    [No Abstract]   [Full Text] [Related]  

  • 2. [TAR syndrome (congenital thrombocytopenia and aplasia of the radial bones) in a 5-months-old boy].
    Midro AT; Iwaszkiewicz-Pawłowska A; Puchnarewicz A; Debek K
    Wiad Lek; 1992 Jan; 45(1-2):66-9. PubMed ID: 1295244
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Genetic morphological fatal syndromes. The Fryns syndrome].
    Henkel KE; Pfeiffer RA; Stöss H
    Pathologe; 1993 Mar; 14(2):92-3. PubMed ID: 8469652
    [No Abstract]   [Full Text] [Related]  

  • 4. [A familial case of Rothmund-Thomson syndrome. A case in favor of the uniqueness of the syndrome. Association with osteosarcoma].
    Rebaud P; David L; Plauchu H; Chatelain P; Moulin G; François R
    Pediatrie; 1985 Sep; 40(6):487-92. PubMed ID: 3869684
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Two new cases of thrombocytopenia absent radius (TAR) syndrome: clinical, genetic and nosologic features.
    Giuffrè L; Cammarata M; Corsello G; Vitaliti SM
    Klin Padiatr; 1988; 200(1):10-4. PubMed ID: 3367608
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Tetraphocomelia in the syndrome of thrombocytopenia with absent radii (TAR syndrome).
    Anyane-Yeboa K; Jaramillo S; Nagel C; Grebin B
    Am J Med Genet; 1985 Apr; 20(4):571-6. PubMed ID: 3993682
    [TBL] [Abstract][Full Text] [Related]  

  • 7. LADD syndrome in five members of a three-generation family and prenatal diagnosis.
    Francannet C; Vanlieferinghen P; Dechelotte P; Urbain MF; Campagne D; Malpuech G
    Genet Couns; 1994; 5(1):85-91. PubMed ID: 8031542
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Association of atrial-ventricular septal defect, blepharophimosis, anal and radial defects in sibs: a new syndrome?
    Houlston RS; Ironton R; Temple IK
    Genet Couns; 1994; 5(1):93-6. PubMed ID: 8031543
    [No Abstract]   [Full Text] [Related]  

  • 9. Antley-Bixler syndrome: case report and review of the literature.
    Poddevin F; Delobel B; Courreges P; Bayart M
    Genet Couns; 1995; 6(3):241-6. PubMed ID: 8588853
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A lethal, unclassifiable form of micromelic dwarfism with posterior cleft palate, multiple cervicothoracal vertebral anomalies and iliac hypoplasia: evidence for autosomal recessive inheritance.
    Fryns JP; Moerman P
    Genet Couns; 1998; 9(1):61-2. PubMed ID: 9555592
    [No Abstract]   [Full Text] [Related]  

  • 11. [Roberts-SC phocomelia syndrome].
    Kawame H
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):234-5. PubMed ID: 11057210
    [No Abstract]   [Full Text] [Related]  

  • 12. [Roberts-SC phocomelia syndrome].
    Musfeld DA; Bühler EM; Heinzl S
    Gynakol Geburtshilfliche Rundsch; 2001; 41(1):3-7. PubMed ID: 11423730
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Zinsser-Cole-Engman syndrome. Apropos of 2 cases of dominant autosomic transmission].
    Gasparini G; Sambvani N; Guidarelli C; Sarchi G; Di Pietro A; Raimondi E; Romagnoni MM; Stefanini M
    G Ital Dermatol Venereol; 1985; 120(6):429-33. PubMed ID: 4086056
    [No Abstract]   [Full Text] [Related]  

  • 14. [Roberts' syndrome. Review of the literature and presentation of 2 clinical cases].
    Colombo B; Bottelli A; Maserati E
    Pediatr Med Chir; 1986; 8(3):411-3. PubMed ID: 3786205
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Rothmund-Thomson syndrome, trisomy 8 mosaicism and RECQ4 gene mutation].
    Durand F; Castorina P; Morant C; Delobel B; Barouk E; Modiano P
    Ann Dermatol Venereol; 2002; 129(6-7):892-5. PubMed ID: 12218919
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A new syndrome of aphalangy, hemivertebrae, and urogenital-intestinal dysgenesis.
    Johnson VP; Munson DP
    Clin Genet; 1990 Nov; 38(5):346-52. PubMed ID: 2282714
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal detection of Roberts-SC phocomelia syndrome: report of 2 sibs with characteristic manifestations.
    Robins DB; Ladda RL; Thieme GA; Boal DK; Emanuel BS; Zackai EH
    Am J Med Genet; 1989 Mar; 32(3):390-4. PubMed ID: 2658590
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Rothmund-Thomson syndrome in a young man without cataract involvement.
    Esfandiarpoor I; Shamsadini S; Farajzadeh S
    East Mediterr Health J; 2004; 10(1-2):225-7. PubMed ID: 16201731
    [No Abstract]   [Full Text] [Related]  

  • 19. New autosomal dominant radial ray hypoplasia syndrome.
    Goldblatt J; Viljoen D
    Am J Med Genet; 1987 Nov; 28(3):647-54. PubMed ID: 3425633
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Rothmund-Thomson syndrome.
    Vennos EM; James WD
    Dermatol Clin; 1995 Jan; 13(1):143-50. PubMed ID: 7712640
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.