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Journal Abstract Search

241 related items for PubMed ID: 11810654

  • 1.
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  • 2. 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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  • 3. 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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  • 5. [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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  • 7. Prenatal diagnosis of partial monosomy 5p (5p15.1→pter) and partial trisomy 7p (7p15.2→pter) associated with cystic hygroma, abnormal skull development, and ventriculomegaly.
    Chen CP, Wang LK, Chern SR, Wu PS, Ko K, Chen YN, Chen SW, Lee MS, Wang W.
    Taiwan J Obstet Gynecol; 2016 Aug; 55(4):591-5. PubMed ID: 27590389
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  • 9. A three-generation family with terminal microdeletion involving 5p15.33-32 due to a whole-arm 5;15 chromosomal translocation with a steady phenotype of atypical cri du chat syndrome.
    Elmakky A, Carli D, Lugli L, Torelli P, Guidi B, Falcinelli C, Fini S, Ferrari F, Percesepe A.
    Eur J Med Genet; 2014 Mar; 57(4):145-50. PubMed ID: 24556499
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  • 10. Amelioration of the typical cognitive phenotype in a patient with the 5pter deletion associated with Cri-du-chat syndrome in addition to a partial duplication of CTNND2.
    Sardina JM, Walters AR, Singh KE, Owen RX, Kimonis VE.
    Am J Med Genet A; 2014 Jul; 164A(7):1761-4. PubMed ID: 24677774
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  • 11. Prenatal sonographic diagnosis of isolated fetal ascites in cri-du-chat (5p-) syndrome: A case report.
    Cardoso MC, Raposo MI, Ormonde M, Monteiro R, Sampaio A, Cosme P, Mota-Vieira L.
    J Clin Ultrasound; 2019 May; 47(4):232-234. PubMed ID: 30511740
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  • 13. Prenatal detection of cri du chat syndrome on uncultured amniocytes using fluorescence in situ hybridization (FISH).
    Pettenati MJ, Hayworth R, Cox K, Rao PN.
    Clin Genet; 1994 Jan; 45(1):17-20. PubMed ID: 8149646
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  • 16. 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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  • 17. 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 Apr 01; 44(4):101-4. PubMed ID: 10703584
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  • 18. Goldenhar and cri-du-chat syndromes: a contiguous gene deletion syndrome?
    Choong YF, Watts P, Little E, Beck L.
    J AAPOS; 2003 Jun 01; 7(3):226-7. PubMed ID: 12825068
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  • 19. Characterization of a complex chromosomal rearrangement in a patient with a typical catlike cry and no other clinical findings of cri-du-chat syndrome.
    Sreekantaiah C, Kronn D, Marinescu RC, Goldin B, Overhauser J.
    Am J Med Genet; 1999 Sep 17; 86(3):264-8. PubMed ID: 10482877
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  • 20. FISH analysis of terminal deletions in patients diagnosed with cri-du-chat syndrome.
    Marinescu RC, Johnson EI, Grady D, Chen XN, Overhauser J.
    Clin Genet; 1999 Oct 17; 56(4):282-8. PubMed ID: 10636446
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