BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

241 related articles for article (PubMed ID: 10319203)

  • 1. A patient with VACTERL association, amelia and hemifacial microsomia.
    Aftimos S; Winship I
    Clin Dysmorphol; 1999 Apr; 8(2):135-7. PubMed ID: 10319203
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Overlap between VACTERL and hemifacial microsomia illustrating a spectrum of malformations seen in axial mesodermal dysplasia complex (AMDC).
    Bergmann C; Zerres K; Peschgens T; Senderek J; Hörnchen H; Rudnik-Schöneborn S
    Am J Med Genet A; 2003 Aug; 121A(2):151-5. PubMed ID: 12910495
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A fetus with hemifacial microsomia and sirenomelia. The same mesodermal defect spectrum?
    López-Valdez JA; Estrada-Juárez H; Moreno-Verduzco ER; Aguinaga-Ríos M
    Fetal Pediatr Pathol; 2013 Apr; 32(2):152-7. PubMed ID: 22643051
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Four cases of amelia of the upper limb associated with anal atresia--is this VACTERL with extreme limb involvement?
    Price SM; Berry AC; Raymond FL; Turnpenny P; Young ID
    Clin Dysmorphol; 1998 Jan; 7(1):35-40. PubMed ID: 9546828
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A dental and facial anomaly not previously reported with VACTERL association: report of case.
    Topper DC; Zallen RD; Kluender RL
    ASDC J Dent Child; 1990; 57(3):216-9. PubMed ID: 2345216
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Report of a girl with vacterl syndrome and right pulmonary agenesis.
    Avcu S; Akgun C; Temel H; Arslan S; Akbayram S; Unal O
    Genet Couns; 2009; 20(4):379-83. PubMed ID: 20162874
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Hemifacial microsomia. Description of a case with associated rare multiple visceral anomalies].
    Lapetina F; Romano A; Teza F; Piantoni G
    Pediatr Med Chir; 1985; 7(3):467-70. PubMed ID: 3837211
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Oculoauriculovertebral spectrum with radial defects: a new syndrome or an extension of the oculoauriculovertebral spectrum? Report of fourteen Brazilian cases and review of the literature.
    Vendramini S; Richieri-Costa A; Guion-Almeida ML
    Eur J Hum Genet; 2007 Apr; 15(4):411-21. PubMed ID: 17290277
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Interrelationships of the hemifacial microsomia-VATER, VATER, and sirenomelia phenotypes.
    Duncan PA; Shapiro LR
    Am J Med Genet; 1993 Aug; 47(1):75-84. PubMed ID: 8368258
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Oculoauriculovertebral dysplasia (author's transl)].
    Wagner IU; Wimmer M; Probst P
    Klin Padiatr; 1978 Mar; 190(2):209-13. PubMed ID: 417212
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Unilateral Potter syndrome with amelia.
    Barta L; Balogh L; Szinay G; Regöly-Mérei A
    Acta Paediatr Acad Sci Hung; 1981; 22(3):195-9. PubMed ID: 7304159
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Oculoauriculovertebral abnormalities in children of diabetic mothers.
    Ewart-Toland A; Yankowitz J; Winder A; Imagire R; Cox VA; Aylsworth AS; Golabi M
    Am J Med Genet; 2000 Feb; 90(4):303-9. PubMed ID: 10710228
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Oculo-auriculo-vertebral spectrum in Klinefelter syndrome.
    Garavelli L; Virdis R; Donadio A; Sigorini M; Banchini G; Balestrazzi P; Fryns JP
    Genet Couns; 1999; 10(3):321-4. PubMed ID: 10546106
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Goldenhar syndrome and hemifacial microsomia: observations on three patients.
    Thomas P
    Eur J Pediatr; 1980 May; 133(3):287-92. PubMed ID: 7389743
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Bronchial anomalies in VACTERL association.
    Kanu A; Tegay D; Scriven R
    Pediatr Pulmonol; 2008 Sep; 43(9):930-2. PubMed ID: 18671276
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Association between "plagiocephaly" and hemifacial microsomia.
    Padwa BL; Bruneteau RJ; Mulliken JB
    Am J Med Genet; 1993 Dec; 47(8):1202-7. PubMed ID: 8291557
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Goldenhar's syndrome associated with multiple congenital abnormalities.
    Bayraktar S; Bayraktar ST; Ataoglu E; Ayaz A; Elevli M
    J Trop Pediatr; 2005 Dec; 51(6):377-9. PubMed ID: 16186139
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Concordance of prune belly syndrome and VACTERL association].
    Oztürk B; Weber HP; Ganz A
    Klin Padiatr; 1994; 206(5):406-9. PubMed ID: 7799620
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Oculo-auriculo-vertebral spectrum: clinical and molecular analysis of 51 patients.
    Beleza-Meireles A; Hart R; Clayton-Smith J; Oliveira R; Reis CF; Venâncio M; Ramos F; Sá J; Ramos L; Cunha E; Pires LM; Carreira IM; Scholey R; Wright R; Urquhart JE; Briggs TA; Kerr B; Kingston H; Metcalfe K; Donnai D; Newman WG; Saraiva JM; Tassabehji M
    Eur J Med Genet; 2015 Sep; 58(9):455-65. PubMed ID: 26206081
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The CHARGE association in a newborn infant.
    Akisü M; Ozkinay F; Ozyürek R; Küçüktaş A; Kültürsay N
    Turk J Pediatr; 1998; 40(2):283-7. PubMed ID: 9714686
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.