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Journal Abstract Search

77 related items for PubMed ID: 1488975

  • 1. Portohepatic shunt in a Down syndrome patient with an interchange trisomy 47,XY,-2,+der(2),+der(21)t(2;21)(p13;q22.1)mat.
    Kieran MW, Vekemans M, Robb LJ, Sinsky A, Outerbridge EW, Der Kaloustian VM.
    Am J Med Genet; 1992 Oct 01; 44(3):288-92. PubMed ID: 1488975
    [Abstract] [Full Text] [Related]

  • 2. Association between Down syndrome and portohepatic shunt.
    Courtens W, Segers V, Johansson A, Avni FE.
    Am J Med Genet; 2000 Jul 17; 93(2):166-8. PubMed ID: 10869124
    [No Abstract] [Full Text] [Related]

  • 3. Interchange trisomy 21 by t(1;21)(p22;q22)mat.
    Dominguez MG, Rivera H, Vasquez AI, Hernández-Zaragoza G, Rivas F.
    Genet Couns; 2001 Jul 17; 12(4):363-7. PubMed ID: 11837606
    [Abstract] [Full Text] [Related]

  • 4. Down syndrome consequent to a cryptic maternal 12p;21q chromosome translocation.
    Scott JA, Wenger SL, Steele MW, Chakravarti A.
    Am J Med Genet; 1995 Mar 13; 56(1):67-71. PubMed ID: 7747789
    [Abstract] [Full Text] [Related]

  • 5. Abnormalities of the umbilico-portal venous system in Down syndrome: a report of two new patients.
    Pipitone S, Garofalo C, Corsello G, Mongiovì M, Piccione M, Maresi E, Sperandeo V.
    Am J Med Genet A; 2003 Aug 01; 120A(4):528-32. PubMed ID: 12884433
    [Abstract] [Full Text] [Related]

  • 6. Cytogenetic analysis of 1572 cases of Down syndrome: a report of double aneuploidy and novel findings 47,XY, t(14;21)(q13;q22.3)mat,+21 and 45,XX,t(14;21) in an Indian population.
    Mandava S, Koppaka N, Bhatia V, Das BR.
    Genet Test Mol Biomarkers; 2010 Aug 01; 14(4):499-504. PubMed ID: 20642367
    [Abstract] [Full Text] [Related]

  • 7. Congenital extrahepatic portocaval shunt (Abernethy type 2), huge liver mass, and patent ductus arteriosus--a case report of its rare clinical presentation in a young girl.
    Kanamori Y, Hashizume K, Kitano Y, Sugiyama M, Motoi T, Tange T.
    J Pediatr Surg; 2003 Apr 01; 38(4):E15. PubMed ID: 12677602
    [Abstract] [Full Text] [Related]

  • 8. [Multiple chromosome aberrations in 3 generations of a family and Down's syndrome resulting from partial trisomy of chromosome 21 (q21--q22)].
    Butomo IV, Prozorova MV, Khitrikova LE.
    Tsitol Genet; 1984 Apr 01; 18(3):223-8. PubMed ID: 6235655
    [Abstract] [Full Text] [Related]

  • 9. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.
    Tüysüz B, Hacihanefioglu S, Silahtaroglu A, Yilmaz S, Deviren A, Cenani A.
    Genet Couns; 2000 Apr 01; 11(4):355-61. PubMed ID: 11140413
    [Abstract] [Full Text] [Related]

  • 10. TIPS in patients with cranial porta hepatis: ultrasound-guided transhepatic portohepatic-portocaval puncture in single needle pass.
    Liang HL, Liu WC, Huang JS, Chen MC, Lai KH, Pan HB, Chen CK.
    AJR Am J Roentgenol; 2011 Apr 01; 196(4):914-8. PubMed ID: 21427345
    [Abstract] [Full Text] [Related]

  • 11. Down syndrome with unusual chromosome translocation: case report and review.
    Bruni L, Capolino R, Tozzi MC, Colloridi F, Smacchia MP.
    Ann Genet; 1996 Apr 01; 39(4):240-2. PubMed ID: 9037352
    [Abstract] [Full Text] [Related]

  • 12. A patient with Down syndrome with a de novo derivative chromosome 21.
    Cetin Z, Yakut S, Mihci E, Manguoglu AE, Berker S, Keser I, Luleci G.
    Gene; 2012 Oct 10; 507(2):159-64. PubMed ID: 22827956
    [Abstract] [Full Text] [Related]

  • 13. Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome.
    El-Ruby M, Hemly NA, Zaki MS.
    Genet Couns; 2007 Oct 10; 18(2):217-26. PubMed ID: 17710874
    [Abstract] [Full Text] [Related]

  • 14. A de novo reciprocal t(2;18) translocation with regular trisomy 21.
    Cyrus C, Kaur H, Koshy T, Thankanadar J, Nallathambi C.
    Genet Test; 2007 Oct 10; 11(4):459-62. PubMed ID: 18294065
    [Abstract] [Full Text] [Related]

  • 15. An unusual portal-systemic shunt, most likely through a patent ductus venosus. A case report.
    Ohnishi K, Hatano H, Nakayama T, Kohno K, Okuda K.
    Gastroenterology; 1983 Oct 10; 85(4):962-5. PubMed ID: 6884718
    [Abstract] [Full Text] [Related]

  • 16. Congenital extrahepatic portocaval shunt: growth in vain.
    Velayutham P, Dev A, Arora A.
    J Pediatr; 2013 May 10; 162(5):1076.e1. PubMed ID: 23295141
    [No Abstract] [Full Text] [Related]

  • 17. Complications of congenital portosystemic shunts in children: therapeutic options and outcomes.
    Franchi-Abella S, Branchereau S, Lambert V, Fabre M, Steimberg C, Losay J, Riou JY, Pariente D, Gauthier F, Jacquemin E, Bernard O.
    J Pediatr Gastroenterol Nutr; 2010 Sep 10; 51(3):322-30. PubMed ID: 20601902
    [Abstract] [Full Text] [Related]

  • 18. Intrahepatic portosystemic venous shunt: diagnosis by color Doppler imaging.
    Kudo M, Tomita S, Tochio H, Minowa K, Todo A.
    Am J Gastroenterol; 1993 May 10; 88(5):723-9. PubMed ID: 8480738
    [Abstract] [Full Text] [Related]

  • 19. [Hypergalactosaemia by congenital portosystemic venous shunt].
    Muramatsu A, Ban K, Wada Y.
    Ryoikibetsu Shokogun Shirizu; 1998 May 10; (18 Pt 1):27-9. PubMed ID: 9589980
    [No Abstract] [Full Text] [Related]

  • 20. Congenital extrahepatic portosystemic venous shunt: imaging features.
    Kandpal H, Sharma R, Arora NK, Gupta SD.
    Singapore Med J; 2007 Sep 10; 48(9):e258-61. PubMed ID: 17728955
    [Abstract] [Full Text] [Related]

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