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Journal Abstract Search

248 related items for PubMed ID: 3577468

  • 1. Prenatal morphology of partial monosomy 18q.
    Lazjuk G, Zolotukhina T, Kirillova I, Lurie I, Novikova I, Abasheva G.
    Zentralbl Gynakol; 1987; 109(2):126-9. PubMed ID: 3577468
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  • 5. Unbalanced 18q/21q translocation in a patient previously reported as monosomy 21.
    Riegel M, Hargreaves P, Baumer A, Guc-Scekic M, Ignjatovic M, Schinzel A.
    Eur J Med Genet; 2005; 48(2):167-74. PubMed ID: 16053908
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  • 8. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
    Chen CP, Chern SR, Wang W, Lee CC, Chen WL, Chen LF, Chang TY, Tzen CY.
    Prenat Diagn; 2001 May; 21(5):346-50. PubMed ID: 11360273
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  • 9. A paternal balanced translocation [t(7;22)(q32;q13.3)] leading to reciprocal unbalanced karyotypes in two consecutive pregnancies.
    Zackowski JL, Raffel LJ, McDaniel LD, Schwartz S.
    Ann Genet; 1990 May; 33(2):113-6. PubMed ID: 2241085
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  • 12. Recurrent proximal 18p monosomy and 18q trisomy in a family with a maternal pericentric inversion of chromosome 18.
    Prabhakara K, Wyandt HE, Huang XL, Prasad KS, Ramadevi AR.
    Ann Genet; 2004 May; 47(3):297-303. PubMed ID: 15337476
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  • 13. Prenatal diagnosis of pure distal 18q deletion.
    Chen CP, Chern SR, Hung FY, Hsu CY, Chang TY, Lee CC, Town DD, Chen WL, Chen LF, Tzen CY, Wang W, Ma R.
    Prenat Diagn; 2006 Feb; 26(2):184-5. PubMed ID: 16470512
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  • 14. Trisomy/partial monosomy 13 mosaicism associated with relatively mild clinical malformation.
    Duckett DP, Porter HJ, Young ID.
    Ann Genet; 1992 Feb; 35(2):113-6. PubMed ID: 1524408
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  • 16. Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 --> pter) and partial monosomy 9p (9p22 --> pter).
    Chen CP, Lin SP, Lin CC, Li YC, Hsieh LJ, Chern SR, Lee CC, Chen YJ, Wang W.
    Prenat Diagn; 2005 Dec; 25(12):1170-2. PubMed ID: 16315335
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  • 18. [Monosomy 7qter (author's transl)].
    Turleau C, de Grouchy J, Perignon F, Lenoir G.
    Ann Genet; 1979 Dec; 22(4):242-4. PubMed ID: 317790
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  • 19. Fetal anomalies associated with an inversion duplication 13 chromosome.
    Rijhsinghani AG, Hruban RH, Stetten G.
    Obstet Gynecol; 1988 Jun; 71(6 Pt 2):991-4. PubMed ID: 3287254
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  • 20. [9p monosomy. About a new case. Clinical and cytogenetic study (author's transl)].
    Lajarrige C, Bouquier JJ, Ronayette D, Tchertoff C, Faugeras C, Barthe D, Laleu J.
    Ann Pediatr (Paris); 1979 Nov; 26(9):631-6. PubMed ID: 555637
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