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PUBMED FOR HANDHELDS

Journal Abstract Search


307 related items for PubMed ID: 7196856

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  • 3. Cri-du-chat syndrome: clinical profile and prenatal diagnosis.
    Tullu MS, Muranjan MN, Sharma SV, Sahu DR, Swami SR, Deshmukh CT, Bharucha BA.
    J Postgrad Med; 1998; 44(4):101-4. PubMed ID: 10703584
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  • 7. De novo appearance of a translocation t(5p; 2Iq), and its transmission in both balanced and unbalanced forms to the next generation.
    Chaganti RS, Morillo-Cucci G, Friis L, Degnan M, German J.
    Ann Genet; 1976 Mar; 19(1):43-8. PubMed ID: 1084121
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  • 12. [Cri-du-chat syndrome and two other deformed children in a family carrying a pericentric inversion or insertion of chromosome 5].
    Delozier-Blanchet CD, Pitmon D, Schorderet D, Engel E.
    J Genet Hum; 1985 Dec; 33(5):371-80. PubMed ID: 4093767
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  • 13. [Prenatal diagnoses in a family with pericentric inversion of chromosome no. 5].
    Körner H, Degen B, Röse I, Metschkarski S.
    Zentralbl Gynakol; 1983 Dec; 105(14):934-9. PubMed ID: 6624295
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  • 16. Cri du chat syndrome after preimplantation genetic diagnosis for reciprocal translocation.
    Ye Y, Luo Y, Qian Y, Xu C, Jin F.
    Fertil Steril; 2011 Jul; 96(1):e71-5. PubMed ID: 21601848
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  • 19. A 45,XX,-5,-14,+t(5q;14q)mat cri du chat child.
    Bass HN, Sparkes RS, Crandall BF, Galos KJ, Howard J.
    Ann Genet; 1978 Mar; 21(1):56-9. PubMed ID: 308345
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  • 20. [Cytogenetic examination in gynecology and obstetrics].
    Knörr K.
    Med Klin; 1974 Jan 18; 69(3):75-82. PubMed ID: 4274010
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