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Journal Abstract Search

152 related items for PubMed ID: 9623797

  • 41. Making sense of maternal serum screening.
    Lindsay P.
    Nurs Times; ; 90(49):30-2. PubMed ID: 7528377
    [Abstract] [Full Text] [Related]

  • 42. Down's syndrome: current screening techniques.
    White RS.
    South Med J; 1989 Dec; 82(12):1483-6. PubMed ID: 2480649
    [Abstract] [Full Text] [Related]

  • 43. Reducing the need for amniocentesis in women 35 years of age or older with serum markers for screening.
    Haddow JE, Palomaki GE, Knight GJ, Cunningham GC, Lustig LS, Boyd PA.
    N Engl J Med; 1994 Apr 21; 330(16):1114-8. PubMed ID: 7510852
    [Abstract] [Full Text] [Related]

  • 44. A study of the steroid sulfatase gene in families with X-linked ichthyosis using polymerase chain reaction.
    Nomura K, Nakano H, Umeki K, Harada K, Kon A, Tamai K, Sawamura D, Hashimoto I.
    Acta Derm Venereol; 1995 Sep 21; 75(5):340-2. PubMed ID: 8615047
    [Abstract] [Full Text] [Related]

  • 45. Molecular studies of deletions at the human steroid sulfatase locus.
    Shapiro LJ, Yen P, Pomerantz D, Martin E, Rolewic L, Mohandas T.
    Proc Natl Acad Sci U S A; 1989 Nov 21; 86(21):8477-81. PubMed ID: 2813406
    [Abstract] [Full Text] [Related]

  • 46. X-linked ichthyosis: an update.
    Hernández-Martín A, González-Sarmiento R, De Unamuno P.
    Br J Dermatol; 1999 Oct 21; 141(4):617-27. PubMed ID: 10583107
    [Abstract] [Full Text] [Related]

  • 47. Association of undetectable unconjugated estriol on multiple marker screening with steroid sulfatase deficiency.
    Jari SD, Fraer LM, Hogge WA.
    Fetal Diagn Ther; 2004 Oct 21; 19(1):43-8. PubMed ID: 14646417
    [Abstract] [Full Text] [Related]

  • 48. Gene diagnosis in X-linked ichthyosis.
    Herrmann FH, Wirth B, Wulff K, Hadlich J, Voss M, Gillard EF, Kruse TA, Ferguson-Smith MA, Gal A.
    Arch Dermatol Res; 1989 Oct 21; 280(8):457-61. PubMed ID: 2493225
    [Abstract] [Full Text] [Related]

  • 49. Multiple screening for fetal Down's syndrome with the classic triple test, dimeric inhibin A and ultrasound.
    Debiève F, Bouckaert A, Hubinont C, Thomas K.
    Gynecol Obstet Invest; 2000 Oct 21; 49(4):221-6. PubMed ID: 10828702
    [Abstract] [Full Text] [Related]

  • 50. 'Dual positivity' for neural tube defects and down syndrome at maternal serum screening: gestational outcome.
    Zanini R, Tarantini M, Cerri V, Jacobello C, Bellotti D, Lancetti S, Scalchi S, Groli C, Bianchi UA.
    Fetal Diagn Ther; 1998 Oct 21; 13(2):106-10. PubMed ID: 9650657
    [Abstract] [Full Text] [Related]

  • 51. Prenatal diagnosis and variable presentation of recessive X-linked ichthyosis.
    Honour JW, Goolamali SK, Taylor NF.
    Br J Dermatol; 1985 Apr 21; 112(4):423-30. PubMed ID: 3857936
    [Abstract] [Full Text] [Related]

  • 52.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 53. Integrated screening for Down's syndrome based on tests performed during the first and second trimesters.
    Wald NJ, Watt HC, Hackshaw AK.
    N Engl J Med; 1999 Aug 12; 341(7):461-7. PubMed ID: 10441601
    [Abstract] [Full Text] [Related]

  • 54. Maternal serum markers for Down's syndrome pregnancies.
    Chew S, Anandakumar C, Ratnam SS.
    Singapore Med J; 1995 Aug 12; 36(4):417-23. PubMed ID: 8919160
    [Abstract] [Full Text] [Related]

  • 55. X-linked recessive ichthyosis. Enzymatic diagnosis of affected males and female carriers.
    Piraud M, Maire I, Zabot MT.
    Enzyme; 1989 Aug 12; 41(4):227-34. PubMed ID: 2743959
    [Abstract] [Full Text] [Related]

  • 56. [Biochemical diagnosis of X chromosomal ichthyosis].
    Meyer JC, Gilardi S.
    Hautarzt; 1986 Apr 12; 37(4):205-9. PubMed ID: 3457782
    [Abstract] [Full Text] [Related]

  • 57. Diagnosis of a deletion of steroid sulfatase by polymerase chain reaction and high-performance liquid chromatography.
    Sugawara T, Iwaki M, Fujimoto S.
    Clin Chim Acta; 1997 Jul 04; 263(1):25-32. PubMed ID: 9247725
    [Abstract] [Full Text] [Related]

  • 58. Mutation report: a novel partial deletion of exons 2-10 of the STS gene in recessive X-linked ichthyosis.
    Valdes-Flores M, Kofman-Alfaro SH, Vaca AL, Cuevas-Covarrubias SA.
    J Invest Dermatol; 2000 Mar 04; 114(3):591-3. PubMed ID: 10692123
    [Abstract] [Full Text] [Related]

  • 59. An Xp22 microdeletion associated with ocular albinism and ichthyosis: approximation of breakpoints and estimation of deletion size by using cloned DNA probes and flow cytometry.
    Schnur RE, Trask BJ, van den Engh G, Punnett HH, Kistenmacher M, Tomeo MA, Naids RE, Nussbaum RL.
    Am J Hum Genet; 1989 Nov 04; 45(5):706-20. PubMed ID: 2573275
    [Abstract] [Full Text] [Related]

  • 60. Multipoint linkage analysis of steroid sulfatase (X-linked ichthyosis) and distal Xp markers.
    Yates JR, Goudie DR, Gillard EF, Aitken DA, Affara NA, Clayton JF, Tippett PA, Ferguson-Smith MA.
    Genomics; 1987 Sep 04; 1(1):52-9. PubMed ID: 3478297
    [Abstract] [Full Text] [Related]

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