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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

325 related items for PubMed ID: 16215919

  • 41. Prenatal diagnosis of the Meckel syndrome: use of serial ultrasound and alpha-fetoprotein measurements.
    Shapiro LJ, Kaback MM, Toomey KE, Sarti D, Luther P, Cousins L.
    Birth Defects Orig Artic Ser; 1977; 13(3D):267-72. PubMed ID: 72573
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  • 45. Peters anomaly in cri-du-chat syndrome.
    Hope WC, Cordovez JA, Capasso JE, Hammersmith KM, Eagle RC, Lall-Trail J, Levin AV.
    J AAPOS; 2015 Jun; 19(3):277-9. PubMed ID: 26059676
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  • 46. Cri du chat syndrome determined by the 5p15.3-->pter deletion--diagnostic problems.
    Laczmanska I, Stembalska A, Gil J, Czemarmazowicz H, Sasiadek M.
    Eur J Med Genet; 2006 Jun; 49(1):87-92. PubMed ID: 16473315
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  • 50. Molecular cytogenetic characterization of distal 5p deletion syndrome in a fetus with a de novo aberrant chromosome 5 at prenatal diagnosis.
    Chen CP.
    Taiwan J Obstet Gynecol; 2024 Mar; 63(2):266-269. PubMed ID: 38485330
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  • 55. A neuropsychological-genetic profile of atypical cri du chat syndrome: implications for prognosis.
    Cornish KM, Cross G, Green A, Willatt L, Bradshaw JM.
    J Med Genet; 1999 Jul; 36(7):567-70. PubMed ID: 10424821
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  • 59. Cri du chat mosaicism: an unusual case of partial deletion and partial deletion/ duplication of the short arm of chromosome 5, leading to an unusual cri du chat phenotype.
    Murru D, Boccone L, Ristaldi MS, Nucaro AL.
    Genet Couns; 2008 Jul; 19(4):381-6. PubMed ID: 19239081
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