BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

517 related articles for article (PubMed ID: 9788565)

  • 1. Congenital diaphragmatic defects and associated syndromes, malformations, and chromosome anomalies: a retrospective study of 60 patients and literature review.
    Enns GM; Cox VA; Goldstein RB; Gibbs DL; Harrison MR; Golabi M
    Am J Med Genet; 1998 Sep; 79(3):215-25. PubMed ID: 9788565
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Outcomes of congenital diaphragmatic hernia: a population-based study in Western Australia.
    Colvin J; Bower C; Dickinson JE; Sokol J
    Pediatrics; 2005 Sep; 116(3):e356-63. PubMed ID: 16140678
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Associated malformations in cases with congenital diaphragmatic hernia.
    Stoll C; Alembik Y; Dott B; Roth MP
    Genet Couns; 2008; 19(3):331-9. PubMed ID: 18990989
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Associated malformations and chromosomal anomalies in 42 cases of prenatally diagnosed diaphragmatic hernia.
    Witters I; Legius E; Moerman P; Deprest J; Van Schoubroeck D; Timmerman D; Van Assche FA; Fryns JP
    Am J Med Genet; 2001 Nov; 103(4):278-82. PubMed ID: 11746006
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Fryns syndrome--pre and postnatal diagnosis].
    Dix U; Beudt U; Langenbeck U
    Z Geburtshilfe Perinatol; 1991; 195(6):280-4. PubMed ID: 1776320
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Ventral abdominal wall defects--antenatal diagnosis, course of pregnancy and post partum therapy].
    Rabe D; Hendrik HJ; Leucht W; Roth H; Walter C; Schmidt W
    Geburtshilfe Frauenheilkd; 1985 Mar; 45(3):176-82. PubMed ID: 3157611
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Fetal malformations and chromosome abnormalities diagnosed at the Center of Prenatal Diagnosis of the University of Aquila in the 1995-1998 triennium].
    Carta G; Iovenitti P; D'Alfonso A; Mascaretti G; Moscarini M
    Minerva Ginecol; 1999 Oct; 51(10):393-8. PubMed ID: 10638165
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Prenatal diagnosis of the atrioventricular septal defect and it's effect on the outcome of the pregnancies].
    Hajdú J; Beke A; Pete B; Oroszné NJ; Papp Z
    Orv Hetil; 2005 Aug; 146(34):1775-80. PubMed ID: 16184879
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Single gene disorders associated with congenital diaphragmatic hernia.
    Slavotinek AM
    Am J Med Genet C Semin Med Genet; 2007 May; 145C(2):172-83. PubMed ID: 17436300
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [The value of prenatal chromosomal diagnosis in cases of fetal abnormalities: results obtained in 468 pathological pregnancies].
    Vamos E; Elmer C; Lévi S; el Khazen N; Donner C; Avni F; Rodesch F
    Rev Med Brux; 1990 Jun; 11(6):231-5. PubMed ID: 2371470
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal diagnosis and management of congenital heart defect: significance of associated fetal anomalies and prenatal chromosome studies.
    Wladimiroff JW; Stewart PA; Sachs ES; Niermeijer MF
    Am J Med Genet; 1985 Jun; 21(2):285-90. PubMed ID: 3893127
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Congenital abnormalities associated with limb deficiency defects: a population study based on cases from the Hungarian Congenital Malformation Registry (1975-1984).
    Evans JA; Vitez M; Czeizel A
    Am J Med Genet; 1994 Jan; 49(1):52-66. PubMed ID: 8172251
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mosaic tetrasomy 12p: four new cases, and confirmation of the chromosomal origin of the supernumerary chromosome in one of the original Pallister-Mosaic syndrome cases.
    Warburton D; Anyane-Yeboa K; Francke U
    Am J Med Genet; 1987 Jun; 27(2):275-83. PubMed ID: 3605213
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal diagnosis of apparently isolated unilateral multicystic kidney: implications for counselling and management.
    Aubertin G; Cripps S; Coleman G; McGillivray B; Yong SL; Van Allen M; Shaw D; Arbour L
    Prenat Diagn; 2002 May; 22(5):388-94. PubMed ID: 12001193
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Associated malformations in patients with esophageal atresia.
    Stoll C; Alembik Y; Dott B; Roth MP
    Eur J Med Genet; 2009; 52(5):287-90. PubMed ID: 19410022
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The Potter sequence: a clinical analysis of 80 cases.
    Curry CJ; Jensen K; Holland J; Miller L; Hall BD
    Am J Med Genet; 1984 Dec; 19(4):679-702. PubMed ID: 6393764
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Morphological study of the removed fetus after therapeutic abortion for echographic anomalies (apropos of 42 cases)].
    Serville F; Carles D; Mainguene M; Maugey B; Vanga A
    J Genet Hum; 1985 Sep; 33(3-4):301-12. PubMed ID: 3903051
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The fetal dandy walker complex: associated anomalies, perinatal outcome and postnatal imaging.
    Harper T; Fordham LA; Wolfe HM
    Fetal Diagn Ther; 2007; 22(4):277-81. PubMed ID: 17369695
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Prenatal outcome of sex chromosome anomalies diagnosed during pregnancy: a retrospective study of 47 cases].
    Perrotin F; Guichet A; Marret H; Potin J; Body G; Lansac J
    J Gynecol Obstet Biol Reprod (Paris); 2000 Nov; 29(7):668-76. PubMed ID: 11119039
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Fetal chromosome abnormalities diagnosed by chorionic villi sampling].
    Gardó S; Bajnóczky K; Nagy M; Nagy S
    Orv Hetil; 1993 Oct; 134(44):2427-30. PubMed ID: 8233461
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 26.