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Journal Abstract Search

197 related items for PubMed ID: 19495505

  • 1. Prenatal diagnosis of cri-du-chat syndrome: importance of ultrasonographical markers.
    Teoh XH, Tan TY, Chow KK, Lee IW.
    Singapore Med J; 2009 May; 50(5):e181-4. PubMed ID: 19495505
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  • 2. 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; 22(1):64-6. PubMed ID: 11810654
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  • 3. 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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  • 4. Prenatal Diagnosis of 5p Deletion Syndrome with Brain Abnormalities by Ultrasonography and Fetal Magnetic Resonance Imaging: A Case Report.
    Kaymak D, Alpay V, Erenel H, Adaletli İ, Comunoglu N, Madazli R.
    Fetal Pediatr Pathol; 2020 Oct; 39(5):446-451. PubMed ID: 31553256
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  • 5. 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 Oct; 44(4):101-4. PubMed ID: 10703584
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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(7):351-2. PubMed ID: 16215919
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  • 7. 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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  • 8. Fetal choroid plexus cysts in association with cri du chat (5p-) syndrome.
    Sarno AP, Polzin WJ, Kalish VB.
    Am J Obstet Gynecol; 1993 Dec; 169(6):1614-5. PubMed ID: 8267073
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  • 9. [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 Dec; 17(7):1304-8. PubMed ID: 7196856
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  • 10. [The Cri du Chat syndrome: a study on the quality of care].
    Cerruti Mainardi P, Spunton M, Arcuri V, Pastore G, Pedrinazzi M, Nardi S, Castronovo C, Alessi D, Guala A.
    Minerva Pediatr; 2012 Aug; 64(4):395-400. PubMed ID: 22728611
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  • 12. 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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  • 13. De novo unbalanced translocation resulting in monosomy for distal 5p (5p14.1 → pter) and 14q (14q32.31 → qter) associated with fetal nuchal edema, microcephaly, intrauterine growth restriction, and single umbilical artery: prenatal diagnosis and molecular cytogenetic characterization.
    Chen CP, Fu CH, Chern SR, Wu PS, Su JW, Lee CC, Lee MS, Wang W.
    Taiwan J Obstet Gynecol; 2013 Sep; 52(3):401-6. PubMed ID: 24075381
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  • 16. [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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