BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

153 related articles for article (PubMed ID: 22643051)

  • 1. 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]  

  • 2. 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]  

  • 3. Sirenomelia: A Multi-systemic Polytopic Field Defect with Ongoing Controversies.
    Boer LL; Morava E; Klein WM; Schepens-Franke AN; Oostra RJ
    Birth Defects Res; 2017 Jun; 109(10):791-804. PubMed ID: 28509418
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Caudal dysplasia syndrome and sirenomelia: are they part of a spectrum?
    Bruce JH; Romaguera RL; Rodriguez MM; González-Quintero VH; Azouz EM
    Fetal Pediatr Pathol; 2009; 28(3):109-31. PubMed ID: 19365740
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Sirenomelia as a part of VACTERL association: a study of three cases].
    Charlier P; Valat AS; Boute O; Petit S; Chafiotte C; Huynh-Charlier I; Gosselin B; Devisme L
    Ann Pathol; 2008 Jun; 28(3):176-81. PubMed ID: 18706355
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A fetus with sirenomelia, omphalocele, and meningomyelocele, but normal kidneys.
    McCoy MC; Chescheir NC; Kuller JA; Altman GC; Flannagan LM
    Teratology; 1994 Aug; 50(2):168-71. PubMed ID: 7801305
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Sirenomelia and VACTERL association in the offspring of a woman with diabetes.
    Castori M; Silvestri E; Cappellacci S; Binni F; Sforzolini GS; Grammatico P
    Am J Med Genet A; 2010 Jul; 152A(7):1803-7. PubMed ID: 20583159
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Sirenomelia and multicystic renal dysplasia. Apropos of 2 cases].
    Chappard D; Lauras B; Fargier P; Knopf JF
    J Genet Hum; 1983 Dec; 31 Suppl 5():403-11. PubMed ID: 6674416
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Sirenomelia--prenatal diagnosis and clinical consequences of a rare abnormality].
    Heyl W; Funk A; Grün M; Rath W
    Z Geburtshilfe Neonatol; 1998; 202(3):121-6. PubMed ID: 9715528
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Sirenomelia--a rare cause of an oligoanhydramnion in the second trimester--a case report].
    Morfeld CA; Hofstaetter C; Adolf S; Radner H; Schild RL
    Z Geburtshilfe Neonatol; 2012 Feb; 216(1):34-6. PubMed ID: 22331526
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Sirenomelia: An anatomical assessment and genetic sex determination of two cases.
    Vander Pol SL; MacKenzie JJ; Harrison KJ; Reifel CW; Smith RML; Bale L; Pang SC; Taylor SAM
    J Anat; 2024 Jun; 244(6):1093-1101. PubMed ID: 38267217
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Sirenomelia with associated systemic anomalies: an autopsy pathologic illustration of a series of four cases.
    Chikkannaiah P; Mahadevan A; Gosavi M; Kangle R; Anuradha ; Shankar SK
    Pathol Res Pract; 2014 Jul; 210(7):444-9. PubMed ID: 24656289
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Craniorachischisis totalis and sirenomelia.
    Rodríguez JI; Palacios J
    Am J Med Genet; 1992 Jul; 43(4):732-6. PubMed ID: 1621765
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Caudal dysgenesis and sirenomelia-single centre experience suggests common pathogenic basis.
    Thottungal AD; Charles AK; Dickinson JE; Bower C
    Am J Med Genet A; 2010 Oct; 152A(10):2578-87. PubMed ID: 20734338
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [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]  

  • 18. Sirenomelia associated with a "vanishing twin".
    Kapur RP; Mahony BS; Nyberg DA; Resta RG; Shepard TH
    Teratology; 1991 Feb; 43(2):103-8. PubMed ID: 2014475
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Sirenomelia: a case report.
    Mysorekar VV; Rao SG; Sundari N
    Indian J Pathol Microbiol; 2007 Apr; 50(2):359-61. PubMed ID: 17883073
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cebocephaly, alobar holoprosencephaly, spina bifida, and sirenomelia in a stillbirth.
    Chen CP; Shih SL; Liu FF; Jan SW
    J Med Genet; 1997 Mar; 34(3):252-5. PubMed ID: 9132501
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.