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Journal Abstract Search

130 related items for PubMed ID: 18444226

  • 1. Correlation between ultrasound and pathological examination in a prenatal diagnosis of Cri du Chat syndrome associated with partial trisomy 17q.
    Cordier AG, Braidy C, Levaillant JM, Brisset S, Maurin ML, Mas AE, Frydman R, Tachdjian G, Picone O.
    Prenat Diagn; 2008 May; 28(5):463-5. PubMed ID: 18444226
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  • 2. 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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  • 7. [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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  • 8. 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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  • 10. Monosomy 5p and partial trisomy 8q due to maternal balanced translocation.
    Imataka G, Arisaka O.
    Genet Couns; 2013 Sep 17; 24(4):435-7. PubMed ID: 24551988
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  • 11. A yeast artificial chromosome contig of the critical region for cri-du-chat syndrome.
    Goodart SA, Simmons AD, Grady D, Rojas K, Moyzis RK, Lovett M, Overhauser J.
    Genomics; 1994 Nov 01; 24(1):63-8. PubMed ID: 7896290
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  • 12. Clinical and molecular characterization of 12 prenatal cases of Cri-du-chat syndrome.
    Peng Y, Pang J, Hu J, Jia Z, Xi H, Ma N, Yang S, Liu J, Huang X, Tang C, Wang H.
    Mol Genet Genomic Med; 2020 Aug 01; 8(8):e1312. PubMed ID: 32500674
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  • 13. A de novo cryptic 5p deletion and 9p duplication detected by subtelomeric MLPA in a boy with cri du chat syndrome.
    Lincoln-de-Carvalho CR, Vicente FM, Vieira TA, de Mello MP, Marques-de-Faria AP.
    Am J Med Genet A; 2011 Feb 01; 155A(2):450-4. PubMed ID: 21271672
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  • 14. Problem behaviors associated with deletion Prader-Willi, Smith-Magenis, and cri du chat syndromes.
    Clarke DJ, Boer H.
    Am J Ment Retard; 1998 Nov 01; 103(3):264-71. PubMed ID: 9833657
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  • 15. [Cytogenetic and molecular genetic diagnosis of a neonate with partial 13q trisomy and partial 5p monosomy].
    Xiao W, Gao Z, Meng Q, Zhang M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Dec 01; 31(6):747-9. PubMed ID: 25449080
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  • 16. Partial monosomy 5p and partial trisomy 5q due to paternal pericentric inversion of chromosome 5.
    Ono K, Ohashi Y, Nakano H, Togashi H, Kannari Y, Isono S.
    Jpn J Hum Genet; 1993 Sep 01; 38(3):319-28. PubMed ID: 8260723
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  • 17. Prenatal diagnosis of cri-du-chat syndrome: importance of ultrasonographical markers.
    Teoh XH, Tan TY, Chow KK, Lee IW.
    Singapore Med J; 2009 May 01; 50(5):e181-4. PubMed ID: 19495505
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  • 20. [Reverse type of cri du chat disease: 5 p trisomy].
    Stoll C, Rethore MO, Laurent C, Lejeune J.
    Arch Fr Pediatr; 1975 May 01; 32(6):551-61. PubMed ID: 1180635
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