These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

246 related items for PubMed ID: 19241240

  • 1. Congenital perineal hernia in a fetus with trisomy 18.
    Steffensen TS, Opitz JM, Gilbert-Barness E.
    Fetal Pediatr Pathol; 2009; 28(2):95-9. PubMed ID: 19241240
    [Abstract] [Full Text] [Related]

  • 2. Congenital perineal hernia in a fetus with X monosomy.
    Bianca S, Bartoloni G, Barrano B, Boemi G, Barone C, Cataliotti A, Indaco L, Ettore G.
    Congenit Anom (Kyoto); 2009 Dec; 49(4):279. PubMed ID: 20021490
    [No Abstract] [Full Text] [Related]

  • 3. Retroarterial colon with right-sided obstructive gangrenous colitis.
    Murray RA, Craver RD.
    Fetal Pediatr Pathol; 2006 Dec; 25(4):185-9. PubMed ID: 17162525
    [Abstract] [Full Text] [Related]

  • 4. Prenatal diagnosis of trisomy 9.
    Nakagawa M, Hashimoto K, Ohira H, Hamanaka T, Ozaki M, Suehara N.
    Fetal Diagn Ther; 2006 Dec; 21(1):68-71. PubMed ID: 16354979
    [Abstract] [Full Text] [Related]

  • 5. Omphalocele and congenital diaphragmatic hernia associated with fetal trisomy 18.
    Chen CP.
    Prenat Diagn; 2005 May; 25(5):421-3. PubMed ID: 15906414
    [No Abstract] [Full Text] [Related]

  • 6. Perineal hernia: surgical anatomy, embryology, and technique of repair.
    Stamatiou D, Skandalakis JE, Skandalakis LJ, Mirilas P.
    Am Surg; 2010 May; 76(5):474-9. PubMed ID: 20506875
    [Abstract] [Full Text] [Related]

  • 7. First trimester diagnosis of iniencephaly associated with fetal malformations and trisomy 18: report of a new case and gene analysis on folate metabolism in parents.
    Tonni G, Azzoni D, Panteghini M, Ventura A, Cavalli P.
    Congenit Anom (Kyoto); 2007 Sep; 47(3):101-4. PubMed ID: 17688469
    [Abstract] [Full Text] [Related]

  • 8. Trisomy 9 associated with maternal serum screening results positive for trisomy 18. Case report and review of the literature.
    Priola V, De Vivo A, Imbesi G, Azzerboni A, Triolo O.
    Prenat Diagn; 2007 Dec; 27(12):1167-9. PubMed ID: 17828795
    [No Abstract] [Full Text] [Related]

  • 9. Megacystis-microcolon-intestinal hypoperistalsis syndrome and aganglionosis in trisomy 18.
    Chamyan G, Debich-Spicer D, Opitz JM, Gilbert-Barness E.
    Am J Med Genet; 2001 Aug 15; 102(3):293-6. PubMed ID: 11484210
    [Abstract] [Full Text] [Related]

  • 10. A well-documented trisomy 13 case presenting with a number of common and uncommon features of the syndrome.
    Balci S, Güçer S, Orhan D, Karagöz T.
    Turk J Pediatr; 2008 Aug 15; 50(6):595-9. PubMed ID: 19227428
    [Abstract] [Full Text] [Related]

  • 11. Evaluating the incidence and likelihood ratios for chromosomal abnormalities in fetuses with common central nervous system malformations.
    Goetzinger KR, Stamilio DM, Dicke JM, Macones GA, Odibo AO.
    Am J Obstet Gynecol; 2008 Sep 15; 199(3):285.e1-6. PubMed ID: 18771985
    [Abstract] [Full Text] [Related]

  • 12. Trisomy 18 with multiple rare malformations: report of one case.
    Su PH, Chen JY, Hsu CH, Chen SJ, Chan SW, Lin LL.
    Acta Paediatr Taiwan; 2007 Sep 15; 48(5):272-5. PubMed ID: 18254577
    [Abstract] [Full Text] [Related]

  • 13. Congenital perineal hernia: report of a case.
    Mohta A, Bhargava SK.
    Surg Today; 2004 Sep 15; 34(7):630-1. PubMed ID: 15221563
    [Abstract] [Full Text] [Related]

  • 14. Fetal inguinoscrotal hernia: prenatal ultrasound diagnosis and pathogenetic evaluation.
    Paladini D, Palmieri S, Morelli PM, Forleo F, Morra T, Salviati M, Zampella C, D'Angelo A, Martinelli P.
    Ultrasound Obstet Gynecol; 1996 Feb 15; 7(2):145-6. PubMed ID: 8776241
    [Abstract] [Full Text] [Related]

  • 15. The phenotypic spectrum of trisomy 2: report of two new cases.
    Mihci E, Velagaleti GV, Ensenauer R, Babovic-Vuksanovic D.
    Clin Dysmorphol; 2009 Oct 15; 18(4):201-4. PubMed ID: 19474704
    [Abstract] [Full Text] [Related]

  • 16. Ankyloblepharon filiforme adnatum (AFA) associated with trisomy 18.
    Tüysüz B, Ilikkan B, Vural M, Perk Y.
    Turk J Pediatr; 2002 Oct 15; 44(4):360-2. PubMed ID: 12458818
    [Abstract] [Full Text] [Related]

  • 17. Phenotypic expression in the first case of complete trisomy 12: combination of prenatal ultrasound and necropsic examination.
    Machado AP, Ramalho C, Loureiro T, Cunha M, Dória S, Carvalho F, Oliveira JP, Brandão O, Matias A.
    Fetal Diagn Ther; 2009 Oct 15; 25(2):234-8. PubMed ID: 19494495
    [Abstract] [Full Text] [Related]

  • 18. ALOBAR HOLOPROSENCEPHALY, CLEFT LIP/PALATE, URORECTAL SEPTUM MALFORMATION SEQUENCE AND CONGENITAL PERINEAL HERNIA IN A FETUS.
    Girisha KM, Nayak SS, Shukla A, Bhat SK.
    Genet Couns; 2015 Oct 15; 26(3):321-5. PubMed ID: 26625663
    [Abstract] [Full Text] [Related]

  • 19. Sonographic diagnosis of epignathus (oral teratoma), prosencephaly, meromelia and oligohydramnios in a fetus with trisomy 13.
    Yapar EG, Ekici E, Gökmen O.
    Clin Dysmorphol; 1995 Jul 15; 4(3):266-71. PubMed ID: 7551166
    [Abstract] [Full Text] [Related]

  • 20. [Perineal groove--an undiagnosed malformation?].
    Wester T.
    Lakartidningen; 2004 Aug 26; 101(35):2646-7. PubMed ID: 15458218
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 13.