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Journal Abstract Search

306 related items for PubMed ID: 10703584

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. [Prenatal diagnosis of the cri-du-chat syndrome in the case of balanced 5p--; 18p+ translocation in the mother].
    Zolotukhina TV, Butomo IV, Rozovskiĭ IS, Grinberg KN.
    Genetika; 1981; 17(7):1304-8. PubMed ID: 7196856
    [Abstract] [Full Text] [Related]

  • 3. Prenatal diagnosis of minute 5p- deletion: a cytogenetic problem in detection.
    Benn PA, Hsu LY, Verma RS, Alonso ML, Reich E, Wishnick M.
    Obstet Gynecol; 1987 Sep; 70(3 Pt 2):449-52. PubMed ID: 3627600
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  • 4. Prenatal diagnosis of 5p deletion syndrome following abnormally low maternal serum human chorionic gonadotrophin.
    Weiss A, Shalev S, Weiner E, Shneor Y, Shalev E.
    Prenat Diagn; 2003 Jul; 23(7):572-4. PubMed ID: 12868086
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  • 5. [Prenatal detection of crying cat syndrome due to balanced translocation in one parent].
    Barjaktarović N, Pendić B, Garzicić B, Popovic M, Paljm A.
    Nouv Presse Med; 1977 Jan 22; 6(3):180-2. PubMed ID: 834552
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  • 6. Prenatal diagnosis of cri du chat syndrome with encephalocele.
    Bakkum JN, Watson WJ, Johansen KL, Brost BC.
    Am J Perinatol; 2005 Oct 22; 22(7):351-2. PubMed ID: 16215919
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  • 7. 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 22; 96(1):e71-5. PubMed ID: 21601848
    [Abstract] [Full Text] [Related]

  • 8. [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 22; 33(5):371-80. PubMed ID: 4093767
    [Abstract] [Full Text] [Related]

  • 9. Mosaic Cri du Chat syndrome in a patient exhibiting three 5p cell lines.
    Kitsiou S, Kolialexi A, Mavrou A.
    Prenat Diagn; 2004 Jul 22; 24(7):578-9. PubMed ID: 15300755
    [No Abstract] [Full Text] [Related]

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  • 12. Variability in a family with an insertion involving 5p.
    Marinescu RC, Mamunes P, Kline AD, Schmidt J, Rojas K, Overhauser J.
    Am J Med Genet; 1999 Sep 17; 86(3):258-63. PubMed ID: 10482876
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  • 13. 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 Sep 17; 19(4):381-6. PubMed ID: 19239081
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  • 14. [Prognosis in the cri-du-chat syndrome].
    Oosterwijk JC, Verboom AJ, Bijlsma JB.
    Tijdschr Kindergeneeskd; 1987 Dec 17; 55(6):226-33. PubMed ID: 3327195
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  • 15. Two cases of deletion 5p syndrome: one with paternal involvement and another with atypical presentation.
    Azman BZ, Akhir SM, Zilfalil BA, Ankathil R.
    Singapore Med J; 2008 Apr 17; 49(4):e98-e100. PubMed ID: 18418516
    [Abstract] [Full Text] [Related]

  • 16. Dandy-Walker syndrome and corpus callosum agenesis in 5p deletion.
    Vialard F, Robyr R, Hillion Y, Molina Gomes D, Selva J, Ville Y.
    Prenat Diagn; 2005 Apr 17; 25(4):311-3. PubMed ID: 15849798
    [Abstract] [Full Text] [Related]

  • 17. Prenatal diagnosis of cri du chat (5p-) syndrome in association with isolated moderate bilateral ventriculomegaly.
    Stefanou EG, Hanna G, Foakes A, Crocker M, Fitchett M.
    Prenat Diagn; 2002 Jan 17; 22(1):64-6. PubMed ID: 11810654
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  • 19. 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 17; 36(7):567-70. PubMed ID: 10424821
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