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Journal Abstract Search

307 related items for PubMed ID: 7196856

  • 21. [A de novo partial 5p deletion and cryptic 18p duplication detected by SNP-Array in a boy featuring Cri du Chat syndrome].
    Hu JC, Tan K, Cheng DH, Li LY, Lu GX, Tan YQ.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb; 30(1):87-90. PubMed ID: 23450488
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  • 23. Cri-du-chat syndrome diagnosed by amniocentesis performed due to abnormal maternal serum test.
    Fankhauser L, Brundler AM, Dahoun S.
    Prenat Diagn; 1998 Oct; 18(10):1099-100. PubMed ID: 9826907
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  • 25. Wolf-Hirschhorn and Cri du Chat syndromes resulting from familial translocations: 3 further examples of the Bp monosomy epistatic effect.
    Petit P, Fryns JP.
    Genet Couns; 1990 Oct; 1(2):179-84. PubMed ID: 2081002
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  • 26. The "cri du chat" syndrome.
    Mladkovskaya TB, Lebedev BV, Mazaeva IV.
    Sov Genet; 1970 Oct; 6(10):1374-9. PubMed ID: 4272596
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  • 27. 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; 60(2):318-323. PubMed ID: 33678334
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  • 29. Prenatal diagnosis of Cri-du chat syndrome following high maternal serum human chorionic gonodotrophin and ventricular septal defect.
    Li DZ.
    Prenat Diagn; 2009 Sep; 29(9):914. PubMed ID: 19718712
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  • 32. 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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  • 37. [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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