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Journal Abstract Search

147 related items for PubMed ID: 4276810

  • 21.
    ; . PubMed ID:
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  • 22. [Cytogenetics. Importance, limitations and prospects].
    Milani-Comparetti M.
    Minerva Med; 1978 Mar 17; 69(13):885-94. PubMed ID: 148012
    [No Abstract] [Full Text] [Related]

  • 23. Isolated pericardial effusion: an indication for fetal karyotyping?
    Sharland G, Lockhart S.
    Ultrasound Obstet Gynecol; 1995 Jul 17; 6(1):29-32. PubMed ID: 8528797
    [Abstract] [Full Text] [Related]

  • 24.
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  • 25.
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  • 27. Prenatal diagnosis of a 5/15 translocation with 5p and proximal 5q trisomy. Cytogenetic and phenotypic findings.
    Crowder WE, Yeast JD, Falk RE.
    Birth Defects Orig Artic Ser; 1982 Jul 17; 18(3 Pt A):143-51. PubMed ID: 7126787
    [No Abstract] [Full Text] [Related]

  • 28. [Diagnosis of trisomy-21 associated with spina bifida and cheilo-gnatho-palato-schisis during the first trimester of pregnancy].
    Szabó J, Szemere G, Gellén J, Herczeg J.
    Orv Hetil; 1986 Aug 17; 127(33):2015-8. PubMed ID: 2947028
    [No Abstract] [Full Text] [Related]

  • 29. Prenatal diagnosis of partial monosomy 3p and partial trisomy 2p in a fetus associated with shortening of the long bones and a single umbilical artery.
    Chen CP, Liu FF, Jan SW, Lin SP, Lan CC.
    Prenat Diagn; 1996 Mar 17; 16(3):270-5. PubMed ID: 8710784
    [Abstract] [Full Text] [Related]

  • 30.
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  • 31. [Prenatal chromosome analysis in risk fetuses].
    Philip J, Bang J, Hahnemann N, Mikkelsen M, Niebuhr E, Rebbe H, Weber J.
    Ugeskr Laeger; 1974 Jul 15; 136(29):1621-4. PubMed ID: 4276782
    [No Abstract] [Full Text] [Related]

  • 32. Cytogenetic diseases.
    Nyhan WL.
    Clin Symp; 1983 Jul 15; 35(1):1-32. PubMed ID: 6242703
    [No Abstract] [Full Text] [Related]

  • 33. Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization.
    DuPont BR, Huff RW, Ridgway LE, Stratton RF, Moore CM.
    Am J Med Genet; 1994 Mar 01; 50(1):21-7. PubMed ID: 8160748
    [Abstract] [Full Text] [Related]

  • 34. [Prenatal diagnosis of a de novo trisomy case 9q-47,XX,+9 del(q33----qter)].
    Cordier MP, Coicaud C, Thoulon JM, Robert JM, Germain D.
    J Genet Hum; 1984 Dec 01; 32(5):351-61. PubMed ID: 6527131
    [Abstract] [Full Text] [Related]

  • 35. It could be you. Antenatal screening ... just another lottery?
    Rogers J.
    Nurs Times; 1984 Dec 01; 93(6):54-5. PubMed ID: 9095934
    [No Abstract] [Full Text] [Related]

  • 36.
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  • 37. Prenatal diagnosis of interstitial deletion of 17(p11.2p11.2) (Smith-Magenis syndrome).
    Fan YS, Farrell SA.
    Am J Med Genet; 1994 Jan 15; 49(2):253-4. PubMed ID: 8116679
    [No Abstract] [Full Text] [Related]

  • 38. Mid-trimester chorionic biopsy. Case report.
    Szabó J, Gellén J, Szemere G.
    Br J Obstet Gynaecol; 1986 May 15; 93(5):512-3. PubMed ID: 3518790
    [No Abstract] [Full Text] [Related]

  • 39. The prenatal diagnosis of chromosome anomalies.
    Schmid W.
    Triangle; 1972 May 15; 11(3):91-102. PubMed ID: 4656755
    [No Abstract] [Full Text] [Related]

  • 40. [Chromosome studies--introduction to clinical cytogenetics].
    Hansen I.
    Z Allgemeinmed; 1971 Feb 28; 47(6):271-80. PubMed ID: 4255208
    [No Abstract] [Full Text] [Related]

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