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Journal Abstract Search

190 related items for PubMed ID: 834552

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  • 4. [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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  • 6. Cri du chat-syndrome in combination with partial trisomy 9 p.
    Sigmund J, Frisch H, Heinz-Erian P, Rhomberg K, Wegner RD.
    Padiatr Padol; 1986 Dec; 21(1):61-7. PubMed ID: 3960564
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  • 7. [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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  • 8. 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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  • 9. 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 Mar; 44(4):101-4. PubMed ID: 10703584
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  • 11. 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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  • 12. 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; 49(4):e98-e100. PubMed ID: 18418516
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  • 13. Prenatal diagnosis of cri du chat syndrome with encephalocele.
    Bakkum JN, Watson WJ, Johansen KL, Brost BC.
    Am J Perinatol; 2005 Oct; 22(7):351-2. PubMed ID: 16215919
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  • 14. 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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  • 16. Duplication (5p13 leads to pter): prenatal diagnosis and review of the literature.
    Khodr GS, Cadena G, Le KL, Kagan-Hallet KS.
    Am J Med Genet; 1982 May; 12(1):43-9. PubMed ID: 7091195
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  • 17. Identification of a cryptic t(5;7) reciprocal translocation by fluorescent in situ hybridization.
    Bernstein R, Bocian ME, Cain MJ, Bengtsson U, Wasmuth JJ.
    Am J Med Genet; 1993 Apr 01; 46(1):77-82. PubMed ID: 8494035
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  • 18. Prenatal diagnosis of Cri-du-Chat syndrome with concomitant distal trisomy 10q syndrome in one fetus with ultrasound anomalies.
    He JP, Qian Y, Liu WJ, Tang J, Qin MH, Luo SJ, Hou JH, Lv MX.
    Taiwan J Obstet Gynecol; 2021 Mar 01; 60(2):318-323. PubMed ID: 33678334
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  • 19. [Partial monosomy and trisomy 5 p due to balanced translocation t (3,5) in the father (author's transl)].
    Andrle M, Erlach A, Rett A.
    Wien Klin Wochenschr; 1981 Jan 09; 93(1):16-9. PubMed ID: 7222705
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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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